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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881686Generated: November 4, 2026

Dichloromethane → Methyl 4-(1-(naphthalen-1-ylsulfonyl)piperidin-2-yl)butanoate

https://huagongshe.com/reaction/1881686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant4-Methoxy-2,6-dimethylbenzene-1-sulfonyl chlorideHCID 15917496—
ReactantMethyl 4-(piperidin-2-yl)butanoate hydrochlorideHCID 66772062—
ProductMethyl 4-(1-(naphthalen-1-ylsulfonyl)piperidin-2-yl)butanoateHCID 5790426779%

Reaction Steps

The sulfonyl chloride 1 (9.76 g, 85.2 mmol) and Et3N (11.8 ml, 85.2 mmol) were dissolved in CH2Cl2 (100 ml), and a solution of diphenylmethanamine (2, 15.61 g, 85.2 mmol) in CH2Cl2 (40 ml) was added dropwise in the course of 10 min. The reaction mixture was stirred at room temperature for 18 h. The reaction mixture was washed with aqueous 0.5 M KHSO4 (2×200 ml) and sat. NaCl solution (100 ml), dried over Na2SO4 and concentrated to dryness. Recrystallization from CH2Cl2 at 0-5° C. gave 17.63 g (79%) of the sulfonamide 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318769B2
Source datasetuspto-grants-2012_11
ORD IDord-cf7f4129a0f24a0b98daca5c89f6ae79
Source noteuspto-grants-2012_11