Sulfuryl chloride → (R)-3-(2,2-dimethyl-1,3-dioxolan-4-yl)prop-1-ene-2-sulfonyl chloride

HRID 1895535Notes

Reaction equation

C([Li])(C)(C)C.I[C:7](=[CH2:16])[CH2:8][C@@H:9]1[CH2:13][O:12][C:11]([CH3:15])([CH3:14])[O:10]1.[S:17](Cl)([Cl:20])(=[O:19])=[O:18]>CCCCCC.C(OCC)C>[CH3:14][C:11]1([CH3:15])[O:10][C@H:9]([CH2:8][C:7]([S:17]([Cl:20])(=[O:19])=[O:18])=[CH2:16])[CH2:13][O:12]1

Participants

Conditions

Temperature: -78 °C

Procedure

A solution of tert-butyl lithium in hexane (1.7M, 7.65 mL) was added dropwise to a solution of (R)-4-(2-iodoallyl)-2,2-dimethyl-1,3-dioxolane (1.21, 6.5 mmol) in diethyl ether (12 mL) at −78° C., and the reaction stirred at −78° C. for 30 min. Sulfuryl dichloride (SO2Cl2, 538 μL, 6.5 mmol) was added, the mixture warmed to room temperature and the solvents removed under reduced pressure. The product was used in the next step with no further purification.

Workup

temperaturethe mixture warmed to room temperature
customthe solvents removed under reduced pressure
customThe product was used in the next step with no further purification

Sources & evidence

ORD record: ord-d9d91d29dd8e454d97da2c0751b71470
Source dataset: uspto-grants-2013_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08513443B2

Reaction notes

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