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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716303Generated: November 2, 2026

4-(4-Chlorophenoxy)benzene-1-sulfonyl chloride → HCID 59467988, compound

https://huagongshe.com/reaction/1716303

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Chlorophenoxy)benzene-1-sulfonyl chlorideHCID 2757750—
ReactantHCID 68518813HCID 68518813—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 59467988HCID 59467988—

Reaction Steps

To a suspension of (R)-3-amino-1-benzyloxy-piperidin-2-one hydrogen bromide salt (0.086 g, 0.29 mmol) (synthesized according to Miller's procedure J. Org. Chem. 2002, 67, 4759) and 4-(4-chloro-phenoxy)-benzenesulfonyl chloride (0.095 g, 0.31 mmol) in dry CH2Cl2 (3 mL) was treated with TEA (0.12 mL, 0.86 mmol) under N2. The reaction mixture was stirred at room temperature for 6 h and diluted with CH2Cl2 and water. After the usual work-up, the crude material was purified by chromatography (silica gel, 35% EtOAc/hexanes) to give the desired product, (R)—N-(1-Benzyloxy-2-oxo-piperidin-3-yl)-4-(4-chloro-phenoxy)-benzene-sulfonamide. MS (EI) 487 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803793B2
Source datasetuspto-grants-2010_09
ORD IDord-d57a67655e1d4969859a57de19b38b08
Source noteuspto-grants-2010_09