Benzeneacetic acid, 4-bromo- → HCID 14010599, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:16]=[CH:17][C:18]=1[O:19][CH3:20])[CH:6]=[CH:7][C:8]([N:10]1[CH2:15][CH2:14][O:13][CH2:12][CH2:11]1)=[O:9].Br[C:22]1[CH:27]=[CH:26][C:25]([CH2:28][C:29]([OH:31])=[O:30])=[CH:24][CH:23]=1>>[C:29]([CH2:28][C:25]1[CH:26]=[CH:27][C:22](/[C:6](/[C:5]2[CH:16]=[CH:17][C:18]([O:19][CH3:20])=[C:3]([O:2][CH3:1])[CH:4]=2)=[CH:7]/[C:8]([N:10]2[CH2:11][CH2:12][O:13][CH2:14][CH2:15]2)=[O:9])=[CH:23][CH:24]=1)([OH:31])=[O:30]Participants
3
Procedure
This compound was obtained in analogy to the preceding Examples in the form of crystals, m.p. 192°-194° C., from 3,4dimethoxycinnamic acid morpholide and (4-bromophenyl)-acetic acid.
Sources & evidence
- ORD record
- ord-c861ce95fd814b82a7c2844d4c2b0ebd
- Source dataset
- uspto-grants-1990_03
- Patent number
- US04910200
Reaction notes
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