Hydrochloric Acid → 2-(3-Benzyloxyphenyl)-2-chloropropane
Reaction equation
[CH2:1]([O:8][C:9]1[C:10](CCCO)=[CH:11][CH:12]=[CH:13][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[ClH:19].[CH3:20][CH2:21][CH2:22]CCC>>[CH2:1]([O:8][C:9]1[CH:14]=[C:13]([C:21]([Cl:19])([CH3:22])[CH3:20])[CH:12]=[CH:11][CH:10]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
4
Procedure
A mixture of 200 g. (0.826 mole) of 3-benzyloxy-benzene-2-propanol in 50 ml. of hexane and 1 l. of concentrated hydrochloric acid is shaken for 15 minutes in a 2 l. separatory funnel. The organic layer is removed and washed with saturated sodium bicarbonate. The neutralized organic extract is dried over magnesium sulfate and evaporated to give a quantitative yield of the title compound as an oil.
Workup
- additionA mixture of 200 g
- customThe organic layer is removed
- washwashed with saturated sodium bicarbonate
- extractionThe neutralized organic extract
- dry with materialis dried over magnesium sulfate
- customevaporated
Sources & evidence
- ORD record
- ord-2e2e21bb322940d3aaccf110dd625ce9
- Source dataset
- uspto-grants-1989_05
- Patent number
- US04835192
Reaction notes
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