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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964620Generated: October 27, 2026

Methanesulfonyl chloride → 1-(4-Benzyloxy-3-methanesulphonamidophenyl)ethanone

https://huagongshe.com/reaction/964620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1-[3-Amino-4-(benzyloxy)phenyl]ethan-1-oneHCID 15579440—
SolventPyridineHCID 1049—
Product1-(4-Benzyloxy-3-methanesulphonamidophenyl)ethanoneHCID 1236392378%

Reaction Steps

To a mechanically stirred 16° C. pyridine (270 mL) solution of 1-[4-phenylmethoxy-3-aminophenyl]ethanone (57.4 g, 238 mmol) under N2, was added methanesulfonyl chloride (18.6 mL, 240 mmol). After 39 minutes, the completed reaction was quenched with 1.8 L H2O and the resulting suspension stirred for ~2 hours before filtration. The collected solids were washed with H2O (2×250 mL=500 mL) and partially air dried. These solids were dissolved in CHCl3 (450 mL), the aqueous phase removed and heptane (475 mL) added with stirring. The resulting fine suspension was filtered after ~15 minutes, washed with hexane and dried in vacuo at 55° C. to give 59 g (78%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05770615
Source datasetuspto-grants-1998_06
ORD IDord-8f4e7c1944954e5bb24d49dcdd2a6781
Source noteuspto-grants-1998_06