Acetic Acid → HCID 23333206, compound

HRID 1856425Notes

Reaction equation

HRID 1856425 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[C:12]([C:14]([CH3:17])([CH3:16])[CH3:15])[C:11]([OH:18])=[C:10]([C:19]([CH3:22])([CH3:21])[CH3:20])[CH:9]=2)=[CH:4][CH:3]=1.[C:23](O)(=[O:25])[CH3:24].C(OC(=O)C)(=O)C>O>[C:23]([NH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[C:12]([C:14]([CH3:15])([CH3:16])[CH3:17])[C:11]([OH:18])=[C:10]([C:19]([CH3:22])([CH3:21])[CH3:20])[CH:9]=2)=[CH:4][CH:3]=1)(=[O:25])[CH3:24]

Participants

5

Procedure

A solution of 15 g. (0.050 mole) of 4-(4'-aminophenyl)-2,6-di(t-butyl)phenol in 100 ml. of glacial acetic acid is treated with 5.2 g. (0.050 mole) of acetic anhydride. The resulting solution is heated gently for 10 minutes, diluted with water, cooled, and the solid product is separated by filtration. Recrystallization from a benzene-hexane mixture provides 4-(4'-acetamidophenyl)-2,6-di(t-butyl)phenol, m.p. 173°-174.5° C.

Workup

  1. temperatureThe resulting solution is heated gently for 10 minutes
  2. temperaturecooled
  3. customthe solid product is separated by filtration
  4. customRecrystallization from a benzene-hexane mixture

Sources & evidence

ORD record
ord-5d29fc2a8ade408f92fa40bd6f097a9c
Source dataset
uspto-grants-1980_08
Patent number
US04219501

Reaction notes

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