Hydrochloric Acid → HCID 86733512, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][NH:11][C:12]([CH:15]([OH:28])[C:16]2[CH:21]=[CH:20][C:19]([OH:22])=[C:18]([CH2:23][S:24]([CH3:27])(=[O:26])=[O:25])[CH:17]=2)([CH3:14])[CH3:13])=[CH:5][CH:4]=1.[ClH:29]>>[ClH:29].[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:9][CH2:10][NH:11][C:12]([CH:15]([OH:28])[C:16]2[CH:21]=[CH:20][C:19]([OH:22])=[C:18]([CH2:23][S:24]([CH3:27])(=[O:25])=[O:26])[CH:17]=2)([CH3:14])[CH3:13])=[CH:7][CH:8]=1Participants
3
Procedure
The alcohol is treated with hydrogen chloride in methanol-ether giving α-[2-(4-methoxyphenyl)-1,1-dimethylethylaminomethyl]-4-hydroxy-3-(methylsulfonylmethyl)benzyl alcohol hydrochloride as colorless crystals having a melting point of 180°-182°C.
Sources & evidence
- ORD record
- ord-ba8720914f9d488baced56b47b0935de
- Source dataset
- uspto-grants-1976_06
- Patent number
- US03961076
Reaction notes
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