Methanol → HCID 67241392, compound
Reaction equation
[Cl:1][CH2:2][CH2:3][S:4][C:5]1[CH:13]=[CH:12][C:8]([C:9](Cl)=[O:10])=[CH:7][C:6]=1[N+:14]([O-:16])=[O:15].C(N(CC)CC)C.[CH3:24][OH:25]>>[Cl:1][CH2:2][CH2:3][S:4][C:5]1[CH:13]=[CH:12][C:8]([C:9]([O:25][CH3:24])=[O:10])=[CH:7][C:6]=1[N+:14]([O-:16])=[O:15]Participants
4
Procedure
To a solution of 4-(2-chloroethylthio)-3-nitrobenzoyl chloride (22 mg, 0.080 mmol) in MeOH (5 mL) was added triethylamine (0.112 mL, 0.800 mmol). The reaction mixture was allowed to stir for 1 h. TLC analysis of the reaction mixture indicated consumption of starting material. The reaction was concentrated under reduced pressure to provide methyl 4-(2-chloroethylthio)-3-nitrobenzoate (22 mg, 0.080 mmol) as a crude semi-solid, which was used without further purification.
Workup
- customconsumption of starting material
- concentrationThe reaction was concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-f57eabee985f4a99bf32e248a5c1bdc5
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07960376B2
Reaction notes
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