1-Alkenyl-per hydro-indan-4-one derivs. - prepd. by cyclizing 2-(3-alkenyl)-2-cyclohexenone derivs.

    公开(公告)号:DE2440406A1

    公开(公告)日:1976-03-04

    申请号:DE2440406

    申请日:1974-08-23

    Applicant: BASF AG

    Abstract: 1-Alkenyl-per hydro-indan-4-one derivs. of formula (I) (where R1 is H or a satd. or olefinically unsatd. 1-6C aliphatic hydrocarbon residue which can contain oxygen in the form of OH gps. or readily cleavable ether gps; R2 is H or 1-4C alkyl; and one of the broken lines represents an additional C-C bond) e.g. 1-isopropylidene 7a-methylperhydroindan-4-one, are new cpds. (I) are useful as inters. for vitamin D3 and for 17- or 20-keto steroids. (I;R1 = CH3, double bond exocyclic) (Ib) is also useful as an inter. for the alcohol of formula (V) which is an odorant with menthol to camphor-like notes.

    2.
    发明专利
    未知

    公开(公告)号:DE2942646A1

    公开(公告)日:1981-04-30

    申请号:DE2942646

    申请日:1979-10-22

    Applicant: BASF AG

    Abstract: A process for the manufacture of ferromagnetic chromium dioxide modified with foreign elements, by reacting oxides of trivalent and hexavalent chromium under superatmospheric pressure at an elevated temperature in the presence of water and of antimony(III) oxide as modifier, with or without other modifiers in an amount not exceeding 15% by weight, wherein the antimony(III) oxide employed as modifier is, to the extent of more than one-third, present as the senarmontite cubic modification, has a specific surface area, measured by the BET method, of from 1.5 to 15 m2/g, and is added in a total amount of up to 0.5% by weight, based on the resulting chromium dioxide.

    Halo:sulphonyl-thiophene-carboxylic acid prepn. - useful as intermediates for thiophene-saccharin sweetening agents

    公开(公告)号:DE2700261A1

    公开(公告)日:1978-07-13

    申请号:DE2700261

    申请日:1977-01-05

    Applicant: BASF AG

    Abstract: Prepn. of thiophen carboxylic acids of formula (I) is effected by reaction of a 3-ketothiphan carboxylic acid (II) with a sulphonic acid: R4. SO2Y (III) to give a 3-sulphato deriv. then reacting the product with an alkali metal polysulphide. The resulting cpd. is treated with a sulphuric acid chloride or bromide or with Cl2 to give modified polysulphide which is finally treated with ahalogen and water. In the formula R is CO2R3 or H; R2 is H whe R' is -CO2R3; or R' is -CO2R3 when R' is H; R3 is H or an aliphatic group; X is halo; R4 is an aliphatic or aromatic group; Y is halo, the group OR3 or a group -O3S.R4. Provides simple, more economic process for prodn. of (I) which is intermediate for thiophen-saccharin sweetening agents. A typical cpd. methyl-3-chlorosulphonylthiophen-4-carboxylate, was prepd. by the 4-stage process from methyl 3-hydroxy-dihydrothiophen-4-carboxylate.

    1-Alpha-hydroxy-cholesterols prepn - by reducing 1-alpha, 2-alpha-epoxy-3-keto-cpds

    公开(公告)号:DE2400189A1

    公开(公告)日:1975-07-17

    申请号:DE2400189

    申请日:1974-01-03

    Applicant: BASF AG

    Abstract: In a process for the technical prodn. of 1 alpha-hydroxycholesterols of formula (I) (where R1 and R2 are H or OH), e.g., 1 alpha-hydroxy-cholesterol itself, by redn. of 1alpha, 2alpha-epoxy-3-keto-cpds. of formula (II): in liq. NH3, as solvent in the presence of a proton donor, the redn. is carried out with a 2- to 200-fold excess of sodium. (I) are inters. for highly active vitamin D3 derivs. Yields of 50-61.5% are obtd, compared with 45-52% when more expensive Li is used as reducing agent.

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