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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360639Generated: October 29, 2026

Methanesulfonyl chloride → HCID 673827, compound

https://huagongshe.com/reaction/1360639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-(4-Chlorophenyl)ethylamineHCID 67430—
ReactantDiisopropylethylamineHCID 81531—
SolventDichloromethaneHCID 6344—
ProductHCID 673827HCID 67382798.9%

Reaction Conditions

Temperature-5 °C

Reaction Steps

A solution of 4-chlorophenethylamine (5.0 g, 32 mmol) and DIEA (6.0 ml, 35 mmol) in anhydrous DCM (100 ml) was cooled at −5° C. and methanesulfonyl chloride (2.75 ml, 35 mmol) was added dropwise. The resulting mixture was stirred at −5° C. for 1 hour. Then the reaction mixture was washed with a 1N aqueous solution of HCl (2×100 ml) and a saturated aqueous solution of NaHCO3 (100 ml). The aqueous layers were extracted with DCM (100 ml). The organic layers were combined, dried (MgSO4) and the solvent was removed under reduced pressure to give 7.4 g (98%) of the title compound as a pale yellow powder. HPLC, Rt: 2.6 min (purity: 95.1%). LC/MS, M+(ESI): 234.1, M−(ESI): 232.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879876B2
Source datasetuspto-grants-2011_02
ORD IDord-d68bcbfc78684718b6570979e3a89839
Source noteuspto-grants-2011_02