Acetic Anhydride → HCID 13112143, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([Br:8])[CH:5]=[C:4]([Br:9])[C:3]=1[OH:10].[C:11](OC(=O)C)(=[O:13])[CH3:12]>>[C:11]([NH:1][C:2]1[CH:7]=[C:6]([Br:8])[CH:5]=[C:4]([Br:9])[C:3]=1[OH:10])(=[O:13])[CH3:12]Participants
3
Procedure
44.2 g. of 2-amino-4,6-dibromo-phenol were processed with 85.5 ml. of acetic anhydride keeping the temperature under 50° C. By cooling, the 2-acetylamino-4,6-dibromo-phenol separated; it was collected on a filter and crystallized from ethyl alcohol. 30 g. of pure product were obtained. M.P. = 175°-176° C.
Workup
- customunder 50° C
- temperatureBy cooling
- customthe 2-acetylamino-4,6-dibromo-phenol separated
- customit was collected on
- filtrationa filter
- customcrystallized from ethyl alcohol
- customof pure product were obtained
Sources & evidence
- ORD record
- ord-b6cdc5a2298c4e219a11fd25bfdbec78
- Source dataset
- uspto-grants-1978_08
- Patent number
- US04110116
Reaction notes
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