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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471451Generated: November 2, 2026

Methanesulfonyl chloride → HCID 86703886, compound

https://huagongshe.com/reaction/471451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86697154HCID 86697154—
SolventDichloromethaneHCID 6344—
ProductHCID 86703886HCID 8670388664%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(4-Bromo-3,5-dimethyl-phenoxymethyl)-azetidine (400 mg, 1.48 mmol) and DIPEA (0.48 g, 3.7 mmol) are dissolved in 20 mL of dichloromethane and stirred at 0° C. Methanesulfonylchloride (0.12 mL, 1.48 mmol) is added and the reaction mixture is stirred at 0° C. for 2 h. The reaction mixture is washed with water, the organich phase is separated, dried over sodium sulfate and concentrated under vacuum. The crude product is purified by flash chromatography 0-50% ethyl acetate in cyclohexane) to give the title compound (Yield: 330 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633182B2
Source datasetuspto-grants-2014_01
ORD IDord-c1a4a5d9ad174e7183d31fd63fc78435
Source noteuspto-grants-2014_01