Anthraquinone → 1,8-Diamino-2-bromo-4,5-dihydroxy-7-phenoxyanthracene-9,10-dione

HRID 1789318Notes

Reaction equation

HRID 1789318 reaction equation
[NH2:1][C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[C:9]([OH:19])[CH:10]=[C:11]([Br:18])[C:12]=3[NH2:17])[C:7](=[O:20])[C:6]=2[C:5]([OH:21])=[CH:4][C:3]=1Br.C1[C:36]2[C:35](=[O:37])[C:34]3[C:29](=CC=CC=3)[C:28](=O)[C:27]=2C=CC=1>>[NH2:1][C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[C:9]([OH:19])[CH:10]=[C:11]([Br:18])[C:12]=3[NH2:17])[C:7](=[O:20])[C:6]=2[C:5]([OH:21])=[CH:4][C:3]=1[O:37][C:35]1[CH:36]=[CH:27][CH:28]=[CH:29][CH:34]=1

Participants

3

Procedure

When 11.7 g of 1,8-diamino-4,5-dihydroxy-2,7-dibromoanthraquinone (compare Example 350a) are used as the anthraquinone component in Example 415a, then 4.5 g, corresponding to 37% of theory, of 1,8-diamino-4,5-dihydroxy-2-phenoxy-7-bromoanthraquinone are correspondingly obtained. Colour shade on silica gel: blue of Indicator Number 14 (Colour Index Hue Indication Chart).

Sources & evidence

ORD record
ord-7787c3ce113841c98cb4a33921498271
Source dataset
uspto-grants-1987_08
Patent number
US04689171

Reaction notes

Loading…