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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538754Generated: October 28, 2026

4-Toluenesulfonyl chloride → HCID 13355956, compound

https://huagongshe.com/reaction/538754

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
ReactantHCID 53442798HCID 53442798—
SolventDichloromethaneHCID 6344—
ProductHCID 13355956HCID 1335595695.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.200 g (0.97 mmol) of 1-ethyl-4-oxopiperidine-3-carboxylate hydrochloride (commercially available, ABCR) were dissolved in 4 mL of dichloromethane with 0.135 mL (0.97 mmol) of triethylamine. The solution was cooled down to 0° C. and 0.185 g (0.97 mmol) of para-toluenesulfonyl chloride were added followed by 0.135 mL (0.97 mmol) of triethylamine. The reaction was stirred for 20 minutes at 0° C. and overnight at room temperature. Then, the reaction was further diluted with dichloromethane (50 mL) and washed with brine (20 mL×2). The organic layer was dried over Na2SO4 and solvent evaporation gave 300 mg of a white solid (95% yield) which was used for the following step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865758B2
Source datasetuspto-grants-2014_10
ORD IDord-9bbeb38b65e24f93be1a339b5b5f2dfa
Source noteuspto-grants-2014_10