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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737451Generated: October 27, 2026

Triethylamine → HCID 21842580, compound

https://huagongshe.com/reaction/1737451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantN-(2-hydroxy-2-phenylethyl)-N-methylbenzenesulfonamideHCID 21842621—
SolventEthyl AcetateHCID 8857—
ProductHCID 21842580HCID 2184258097%

Reaction Steps

Methanesulfonyl chloride (0.028 mL, 41 mg, 0.36 mmol) was added dropwise over 5 min to a 0° C. solution of N-(2-hydroxy-2-phenylethyl)-N-methylbenzenesulfonamide (100 mg, 0.357 mmol) and triethylamine (0.075 mL, 54 mg, 0.054 mmol) in 1.0 mL of ethyl acetate. After 15 min., the resulting suspension was poured into 40 mL of ice cold ethyl acetate and washed succesively with 20 mL of ice water, 20 mL of ice cold 2.0 N HCl, 20 mL of ice water and 20 mL of brine. The ethyl acetate layer was dried over sodium sulfate and evaporated to give 128 mg of crude N-(2-methanesulfonyloxy-2-phenylethyl)-N-methylbenzenesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962462
Source datasetuspto-grants-1999_10
ORD IDord-747cec38ba114688b22ecc95210adc5f
Source noteuspto-grants-1999_10