-
公开(公告)号:DE2348557A1
公开(公告)日:1975-04-10
申请号:DE2348557
申请日:1973-09-27
Applicant: BASF AG
IPC: C07C101/80
Abstract: The specification is an addition to 2247347 in which 1-amino-anthraquinone-2-carboxylic acid (I) is reacted with CH2O in H2SO4 and the reaction mixt. nitrated to give 1,2-dihydro-6-nitro-7,8-diphthaloyl-3,1,4H-benzoxaz-4-one (II) which is isolated by addn. of a precipitating agent before being hydrolysed by treatment with aq. alkali to give, after acidification pure 1-amino-4-nitro-anthraquinone-2-carboxylic acid (III) as final prod. This process is now modified by using a salt of hydrazine or hydroxylamine as agent for pptn. of (II).
-
公开(公告)号:DE2428337A1
公开(公告)日:1975-12-18
申请号:DE2428337
申请日:1974-06-12
Applicant: BASF AG
Inventor: SCHUHMACHER ALFRED DIPL CHEM D
IPC: C07C97/26
Abstract: 1-amino-2-chloro- and 1-amino-2-bromo-4-hydroxy anthraquinones are prepd. by hydroxylating 1-amino-2:4-dichloro- or 1-amino-2:4-dibromo anthraquinone in H2SO4 in the presence of H3BO4 at 120-170 degrees C, the 2:4-dichloro-or 2:4-dibromo cpd. in the form of a filter cake moist with MeOH, EtOH, or PrOH and contg. at least 50% of the di-halo cpd., is introduced into 100-104.5% H2SO4 contg. 3.5-7% H3BO4, and heated to the reaction temp. i.e. 120-150 degrees C. Used as inters in the prepn. of disperse dyes. The alcohol-wet filter cake is used directly, thus obviating the washing and drying steps of known processes. A pure product is obtained.
-