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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757245Generated: November 2, 2026

Methanesulfonyl chloride → HCID 10711497, compound

https://huagongshe.com/reaction/1757245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 10562764HCID 10562764—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 10711497HCID 10711497—

Reaction Conditions

Temperature0 °C

Reaction Steps

The alcohol described in (b) above (12.6 mg) was dissolved in dichloromethane (2.5 ml) and triethylamine (0.07 ml). This solution was cooled to 0° C. Methanesulfonyl chloride (0.04 ml) was added to the solution dropwise. After stirring for 10 mins the solution was diluted with water and the organic layer was separated, dried (MgSO4), filtered and the solvent removed in vacuo to yield a white solid which was used in the following reaction without further purification. 1H NMR (250 MHz, CDCl3) d 2.44 (3H, s, ArH), 2.94 (3H, s, SO2CH3), 5.51 (2H, s, CH2SO2), 7.08 (1H, d, J=1.5 Hz, imidazole-H), 7.40 (2H, d, J=8.0 Hz, ArH), 7.49 (1H, d, J=1.5 Hz, imidazole-H), 7.92 (2H, d, J=8.0 Hz, ArH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05444074
Source datasetuspto-grants-1995_08
ORD IDord-cf5a752b47f94b74b8fce1d30cc75bbf
Source noteuspto-grants-1995_08