Triethylamine → (2S)-methanesulfonic acid 2-(2,4-difluoro-benzyl)-butyl ester
Reaction equation
[F:1][C:2]1[CH:13]=[C:12]([F:14])[CH:11]=[CH:10][C:3]=1[CH2:4][C@H:5]([CH2:8][CH3:9])[CH2:6][OH:7].C(N(CC)CC)C.[CH3:22][S:23](Cl)(=[O:25])=[O:24]>ClCCl>[F:1][C:2]1[CH:13]=[C:12]([F:14])[CH:11]=[CH:10][C:3]=1[CH2:4][C@H:5]([CH2:8][CH3:9])[CH2:6][O:7][S:23]([CH3:22])(=[O:25])=[O:24]Participants
Conditions
- Temperature
- 0 °C
Procedure
A flask was charged with 7.2 g (36 mmol) of (S)-2-(2,4-difluoro-benzyl)-butan-1-ol and 30 mL of dichloromethane, and the solution was cooled to 0° C. To this solution was added 7.53 mL (54 mmol) of triethylamine, and the mixture was stirred cold for 5 minutes. Then 3.1 mL (39.6 mmol) of methane sulfonyl chloride was added dropwise. The reaction mixture was stirred at room temperature for 16 hours. The dichloromethane was removed under reduced pressure, and the residue was partitioned between 1 N HCl aq. and diethyl ether. The ether layer was collected and washed with sat. aq. sodium bicarbonate, water, and brine. The ether layer was dried over sodium sulfate, filtered, and the ether was removed under reduced pressure. This procedure gave 9.54 g (95% yield) of the titled compound as an orange oil. This material was used without further purification.
Workup
- stirringThe reaction mixture was stirred at room temperature for 16 hours
- customThe dichloromethane was removed under reduced pressure
- customthe residue was partitioned between 1 N HCl aq. and diethyl ether
- customThe ether layer was collected
- washwashed with sat. aq. sodium bicarbonate, water, and brine
- dry with materialThe ether layer was dried over sodium sulfate
- filtrationfiltered
- customthe ether was removed under reduced pressure
Sources & evidence
- ORD record
- ord-c47e758739b94013a1aa32c962e18745
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07179934B2
Reaction notes
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