Ethanone, 1-[3-(2H-benzotriazol-2-yl)-4-hydroxyphenyl]- → HCID 14418975, compound

HRID 1194090Notes

Reaction equation

HRID 1194090 reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:10])[CH3:9])=[CH:4][C:3]=1[N:11]1[N:15]=[C:14]2[CH:16]=[CH:17][CH:18]=[CH:19][C:13]2=[N:12]1.[C:20](OC(=O)C)(=[O:22])[CH3:21].N1C=CC=CC=1>>[C:20]([O:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:10])[CH3:9])=[CH:4][C:3]=1[N:11]1[N:15]=[C:14]2[CH:16]=[CH:17][CH:18]=[CH:19][C:13]2=[N:12]1)(=[O:22])[CH3:21]

Participants

3

Procedure

The crude reaction product 2(2-hydroxy-5-acetylphenyl)2H-benzotriazole (2H5A) is then o-acetylated with an acetic anhydride/pyridine mixture, and after reflux, 2(2-acetoxy-5-acetylphenyl)2H-benzotriazole (2A5A) was produced. The 2(2-acetoxy-5-acetylphenyl)2H-benzotriazole (2A5A) is a key intermediate in the process, and in purified form served as the starting material for the two carbinols.

Sources & evidence

ORD record
ord-8b582f96b2764b2a82be82715979c947
Source dataset
uspto-grants-1989_03
Patent number
US04812575

Reaction notes

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