Hydrochloric Acid → HCID 53897031, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9]CC(C)(C)N=2)=[C:4]([S:15][CH3:16])[C:3]=1[O:17][CH3:18].Cl.[OH2:20]>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([OH:9])=[O:20])=[C:4]([S:15][CH3:16])[C:3]=1[O:17][CH3:18]Participants
4
Procedure
A mixture of 2-[4-chloro-3-methoxy-2-(methylsulphenyl)phenyl]-4,4-dimethyloxazoline (9.0 g) and hydrochloric acid (5M) was stirred and heated at reflux for 5 hours. After cooling, the mixture was diluted with water and extracted with dichloromethane. It was dried (magnesium sulphate), filtered and the filtrate was evaporated to dryness to give 4-chloro-3-methoxy-2-(methylsulphenyl) benzoic acid as a white solid, m.p. 98°-99° C.
Workup
- temperatureheated
- temperatureat reflux for 5 hours
- temperatureAfter cooling
- extractionextracted with dichloromethane
- dry with materialIt was dried (magnesium sulphate)
- filtrationfiltered
- customthe filtrate was evaporated to dryness
Sources & evidence
- ORD record
- ord-49ec3109d7cc465f8a06f4421b1ddaff
- Source dataset
- uspto-grants-1998_09
- Patent number
- US05804532
Reaction notes
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