4-Chlorophenyl chloroformate → (4-Hydroxy-phenyl)-methyl-carbamic acid 4-chloro-phenyl ester
Reaction equation
S([O:5][C:6]1[CH:11]=[CH:10][C:9]([NH:12][CH3:13])=[CH:8][CH:7]=1)(O)(=O)=O.[CH:14]1[C:19]([O:20][C:21](Cl)=[O:22])=[CH:18][CH:17]=[C:16]([Cl:24])[CH:15]=1>>[Cl:24][C:16]1[CH:17]=[CH:18][C:19]([O:20][C:21](=[O:22])[N:12]([C:9]2[CH:10]=[CH:11][C:6]([OH:5])=[CH:7][CH:8]=2)[CH3:13])=[CH:14][CH:15]=1Participants
3
Procedure
In analogy to example 15.1, reaction of 4-methylaminophenol hemisulfate with 4-chlorophenylchloroformate yielded (4-Hydroxy-phenyl)-methyl-carbamic acid 4-chloro-phenyl ester, mp: 143-145° C., dec.; MS: 278 (MH+, 1Cl).
Sources & evidence
- ORD record
- ord-db1c3b80328e40de971e58b82c93fac1
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06683201B2
Reaction notes
Loading…