Methanol → Benzoic acid, 3,5-dichloro-4-methyl-, methyl ester
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([Cl:12])[C:10]=1[CH3:11])[C:5]([OH:7])=[O:6].[CH3:13]O>>[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([Cl:12])[C:10]=1[CH3:11])[C:5]([O:7][CH3:13])=[O:6]Participants
3
Procedure
This compound was prepared in the same manner as in Reference Example 1 (step 1), except that 3,5-dichloro-4-methylbenzoic acid (Japanese Unexamined Patent Publication (Kokai) No. 6-192196) was used and methanol was used as the solvent, and that the crude product was purified by silica gel column chromatography.
Workup
- customthat the crude product was purified by silica gel column chromatography
Sources & evidence
- ORD record
- ord-e51b2b92542745ac848a958d9fc03db1
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07728131B2
Reaction notes
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