2-Chlorobenzoic Acid → HCID 20262575, compound
Reaction equation
Cl[C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH2:11]([O:18][C:19]1[CH:20]=[C:21]([CH:23]=[CH:24][CH:25]=1)[NH2:22])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>>[CH2:11]([O:18][C:19]1[CH:20]=[C:21]([NH:22][C:2]2[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=2[C:4]([OH:6])=[O:5])[CH:23]=[CH:24][CH:25]=1)[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1Participants
3
Procedure
2-(3-Benzyloxyphenylamino)benzoic acid [VII; R and R"=H, OR°=3--OCH2C6H5 ] was prepared from 2-chlorobenzoic acid and 3-benzyloxyaniline according to the procedure of Example 1(a). The green solid obtained was used directly in the next reaction.
Workup
- customThe green solid obtained
- customwas used directly in the next reaction
Sources & evidence
- ORD record
- ord-893f5d1a013e4d0c9db32ca1b9e99e2f
- Source dataset
- uspto-grants-1985_04
- Patent number
- US04510139
Reaction notes
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