Methyl chloroformate → (2-Hydroxymethyl-phenyl)carbamic acid methyl ester
Reaction equation
N[CH:2]([OH:9])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH3:10][O:11][C:12](Cl)=[O:13].CC[N:17](C(C)C)C(C)C>>[CH3:10][O:11][C:12](=[O:13])[NH:17][C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=1[CH2:2][OH:9]Participants
4
Procedure
Reaction of aminobenzylalcohol (3 g) with methylchloroformate (1.9 ml) in the presence of DIPEA (12.8 ml) was performed according to the method described in example 22. The residue was chromatographed on silica gel in dichloromethane/ethyl acetate=25/1 as eluent. Yield: 4.19 g.
Workup
- customThe residue was chromatographed on silica gel in dichloromethane/ethyl acetate=25/1 as eluent
Sources & evidence
- ORD record
- ord-e86d56d26b9943a5a3ca7936ef4d82d8
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08022218B2
Reaction notes
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