PREPARATION OF 4* 5* 6* 77TETRAHYDROOBENZIMIDAZOLINEE22THIONE

    公开(公告)号:JPS54106473A

    公开(公告)日:1979-08-21

    申请号:JP1147378

    申请日:1978-02-06

    Abstract: NEW MATERIAL:A 4, 5, 6, 7-tetrahydro-benzimidazoline-2-thione of formula I: (R is H, alkyl, allyl, or aralkyl group; R is alkyl, allyl, or aralkyl group). EXAMPLE:1-Methyl-4, 5, 6, 7-tetrahydro-benzimidazoline-2-thione. USE:An intermediate for medicines, industrial rubbers or their intermediate, and rust inhibitors. PROCESS:One mole of an 2-amino-cyclohexanone oxime is reacted with 0.5-2 moles, preferably 0.8-1.2 moles of a thiocyanate of formula III in an inert solvent, e.g. benzene, and, without isolation, treated with an acidic substance to form the conpound of formula I.

    NOVEL THIOUREA DERIVATIVE
    3.
    发明专利

    公开(公告)号:JPS54103835A

    公开(公告)日:1979-08-15

    申请号:JP829878

    申请日:1978-01-30

    Abstract: NEW MATERIAL:N-(2-Hydroxyimino-cyclohexyl)-thiourea derivatives of formula I (R is alkyl aryl, aralkyl). EXAMPLE:The compound of formula II. USE:Novel starting materials for medicines, agricultural chemicals, rubber additives, antirusting agents for metals. PREPARATION:In an example, the reaction of 2-amino-cyclohexanone oxime with a thioisocyanate of R-NCS in an inert solvent affords the objective compound of formula I. The 2-amino-cyclohexanone oxime is prepared by a method shown in the reaction equations.

    PRODUCTION OF D-OR L-N2-BENZYLOXYCARBONYL-N6-T-BUTYLOXYCARBONYLLYSINE

    公开(公告)号:JPS6226261A

    公开(公告)日:1987-02-04

    申请号:JP16476285

    申请日:1985-07-25

    Abstract: PURPOSE:To obtain at low cost a high-quality compound useful as a raw material for peptide synthesis, by reacting D- or L-N -benzyloxycarbonyllysine with t-butylphenyl carbonate. CONSTITUTION:D- Or L-N -benzyloxycarbonyllysine is reacted with 6-butylphenyl carbonate in a polar organic solvent such as dimethyl sulfoxide, etc., in the presence of an alkali metal such as hydroxide, carbonate, bicarbonate, etc., of an alkali metal such as K, Na, Li, etc., at 50-100 deg.C to give the aimed substance. The amount of the alkali metallic compound is 1.0-1.2 equivalent based on D- or L-lysine as the starting substance, the amount of t-butylphenyl carbonate is 1.0-1.5mol and the reaction is carried out.

    PRODUCTION OF D-OR L-N2-BENZYLOXYCARBONYL-N6-T-BUTYLOXYCARBONYLLYSINE

    公开(公告)号:JPS61194060A

    公开(公告)日:1986-08-28

    申请号:JP3282685

    申请日:1985-02-22

    Abstract: PURPOSE:To obtain the titled compound useful as a synthetic raw material for peptide, economically, by hydrolyzing D- or L-3-benzyloxycarbonylamino-1-t- butyloxycarbonyl-2-oxohexahydroazepine. CONSTITUTION:The objective D- or L-N -benzyloxycarbonyl-N -t-butyloxy carbonyllysine can be produced by hydrolyzing D- or L-3- benzyloxycarbonylamino-1-t-buthyloxycarbonyl-2-oxohexahydroza epine. The starting compound is obtained easily from the industrial raw material used in the enzymatic production of L-lysine. The hydrolysis is carried out by using lithium hydroxide, etc., keeping the reaction system in alkaline state.

    PREPARATION OF 4* 5* 6* 77TETRAHYDROOBENZIMIDAZOLINEE22THIONE

    公开(公告)号:JPS54106472A

    公开(公告)日:1979-08-21

    申请号:JP1147278

    申请日:1978-02-06

    Abstract: PURPOSE:To obtain the title compound which is an intermediate for medicines in simple procedures in high yield, by treating a specific compound, readily prepared through addition reaction between 2-amino-cyclohexanone oxime and a thioisocyanate, with an acidic substance. CONSTITUTION:A N-(2-hydroxyimino-cyclohexyl)-thiourea of formula I: (R is alkyl, allyl, or aralkyl group) is brought into contact with an acidic substance, e.g. hydrogen chloride, hydrogen bromide, sulfuric or benzenesulfonic acid, at 0- 150 deg.C, preferably 10-100 deg.C to give the objective compound of formula II. The thiourea of formula I is obtained by addition reaction of 2-amino-cyclohexanone oxime with a thiocyanate of formula IV according to the well-known method. Preferably, the amount of the acidic substance is 0.01 mole or more per mole of the compound of formula I.

    NONNELECTROLYTIC COPPER PLATING
    7.
    发明专利

    公开(公告)号:JPS54103748A

    公开(公告)日:1979-08-15

    申请号:JP1080678

    申请日:1978-02-02

    Abstract: PURPOSE:To produce a Cu film excellent in the adhesivity, luster, and color tone with addition of specified imidazole compound to the acid solution in non-electrolytic Cu plating on the iron surface using the acid solution containing Cu ion. CONSTITUTION:With an iron immersed into an acid solution containing CuSO4 or the like in an amount of 0.05 to 8 g/1, preferably 0.1 to 5 g/l, a non-electrolytic Cu plating is applied to the Fe surface under the following condition: Imidazole compound (i.g. 2-mercapto-4, 5, 6, 7-tetrahydrobenzoimidazole and 2-mercaptobenzoimidazole) as shown by the formula I (R represents alkyl group excluding H and C4) and the formula II is allowed to be present at a rate of 0.03 to 0.1 mol per mol of Cu and a plating is performed at a bath temperature of 40 to 80 deg.C for 0.5 to 30 minutes.

    HOT-MELT TYPE ADHESIVE
    8.
    发明专利

    公开(公告)号:JPH07157743A

    公开(公告)日:1995-06-20

    申请号:JP30521593

    申请日:1993-12-06

    Abstract: PURPOSE:To provide the adhesive comprising a powdery material consisting mainly of a nylon having point and the powder of a nylon copolymer copolymerized with nylon 12 in a specificeness amount, having a low melting point, and good in adhesiv and washing resistance. CONSTITUTION:This adhesive comprises (A) 5-40wt.% of a powdery material having a melting point of 80-105 deg.C and consisting mainly of a nylon (preferably a powdery material consisting mainly of the quaternary copolymer of nylon 6/nylon 66/nylon 610/nylon 12) and (B) 95-60wt.% of the powder of a nylon copolymer copolymerized with 30-80wt.% of nylon 12 (preferably the quaternary nylon copolymer of nylon 6/nylon 66/nylon 610/nylon 12). The adhesive is generally prepared by dry-blending the components A and B with each other before coated on a web.

    PRODUCTION OF ALIPHATIC NITRILES
    9.
    发明专利

    公开(公告)号:JPH01104035A

    公开(公告)日:1989-04-21

    申请号:JP26202387

    申请日:1987-10-16

    Abstract: PURPOSE:To obtain the title compound which is used as a starting substance for medicines, agrochemicals, or polymers, with economical advantage, by effecting the reaction between fatty acids and urea in a fused state using a specific catalyst of high activity, without formation of deposits on the wall surfaces of the reactor. CONSTITUTION:The reaction of a fatty acid such as an aliphatic monocarboxylic acid of 6-20 carbon atoms with urea is carried out in a fused state, using a combination of cobalt acetate and boric acid as a catalyst, preferably in a temperature range from 180-210 deg.C at the former stage of the reaction for several hours, then over 220 deg.C, preferably 230-280 deg.C at the latter stage to give the subject compound. The amount of urea used is 1-3mol., preferably 1.01-1.5mol. per mole of the carboxyl group in the fatty acid. The amount of cobalt acetate as the catalyst is 0.1-5wt.%, preferably 0.3-3wt.% and the boric acid is preferably 0.3-3wt.% based on the fatty acid.

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