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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397713Generated: October 27, 2026

Dichloromethane → HCID 23001045, compound

https://huagongshe.com/reaction/397713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantEthanesulfonyl chlorideHCID 11667—
ReactantHCID 23000976HCID 23000976—
SolventPyridineHCID 1049—
ProductAmmoniaHCID 222—
ProductHCID 23001045HCID 23001045119.8%

Reaction Steps

To a solution of 4-(3-aminophenyl)-N-hexyl-4-n-propylpiperidine (Preparation 70, 34 mg, 0.11 mmol) in pyridine (0.5 ml) under nitrogen was added ethanesulfonyl chloride (16 ml, 0.17 mmol) and the resultant mixture was stirred overnight. Ice (2 g) was added and, after 15 min, dichloromethane (3 ml) was added and the biphasic mixture was left to stir for 15 min. The layers were separated and the aqueous layer was extracted with dichloromethane (3 ml). The combined extracts were dried (Na2SO4) and concentrated in vacuo to give the crude product. This was purified by silica (5 g) column chromatography eluting with ethyl acetate:hexane:0.880 ammonia (40:60:1 to 75:25:1) to give the title compound as a pale yellow oil (26 mg, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610711B2
Source datasetuspto-grants-2003_08
ORD IDord-98efeb575e3b4331af759f17f7aa7916
Source noteuspto-grants-2003_08