2-Methyl-3-nitrobenzoic acid → 2-Methyl-3-nitrobenzoyl chloride
Reaction equation
[CH3:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4](O)=[O:5].S(Cl)([Cl:16])=O>>[CH3:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([Cl:16])=[O:5]Participants
3
Procedure
100 g of 2-methyl-3-nitro-benzoic acid and 500 ml of thionyl chloride were refluxed for 15 hours and the mixture was then evaporated to dryness under reduced pressure to obtain 110 g of 2-methyl-3-nitro-benzoyl chloride which was used as in the synthesis.
Workup
- customthe mixture was then evaporated to dryness under reduced pressure
Sources & evidence
- ORD record
- ord-d5171fba49b34619b53dcc9f3a524c2b
- Source dataset
- uspto-grants-1976_01
- Patent number
- US03931302
Reaction notes
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