4-(Benzyloxy)benzoic acid → HCID 67465270, compound
Reaction equation
[Br:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[C:4]([OH:9])[CH:3]=1.[CH2:10]([O:17][C:18]1[CH:26]=[CH:25][C:21]([C:22](O)=O)=[CH:20][CH:19]=1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>>[CH2:10]([O:17][C:18]1[CH:19]=[CH:20][C:21]([C:22]2[O:9][C:4]3[CH:3]=[C:2]([Br:1])[CH:8]=[CH:7][C:5]=3[N:6]=2)=[CH:25][CH:26]=1)[C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1Participants
3
Procedure
Preparation is carried out analogously to 4.1.a from 4-bromo-2-hydroxy-aniline and 4-benzyloxybenzoic acid.
Workup
- customPreparation
Sources & evidence
- ORD record
- ord-613f87a57ae340fb9a73df6b4cdebabc
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08772323B2
Reaction notes
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