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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752020Generated: October 28, 2026

Dichloromethane → 4-[2-(Toluene-4-sulfonyloxymethyl)phenyl]piperidine-1-carboxylic acid t-butyl ester

https://huagongshe.com/reaction/1752020

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantDabcoHCID 9237—
ReactantTert-Butyl 4-(2-(hydroxymethyl)phenyl)piperidine-1-carboxylateHCID 57774474—
SolventEthyl AcetateHCID 8857—
Product4-[2-(Toluene-4-sulfonyloxymethyl)phenyl]piperidine-1-carboxylic acid t-butyl esterHCID 46212988112.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

4-(2-Hydroxymethylphenyl)piperidine-1-carboxylic acid t-butyl ester (0.4 g, 1.0 mmol, 1.0 eq.) and triethylenediamine (220 mg, 2.0 mmol, 1.4 eq.) were dissolved in DCM (11 mL, 170 mmol). The mixture was cooled at 0° C. under nitrogen, TsCl (290 mg, 1.5 mmol, 1.1 eq.) was added, and the mixture was stirred at 0° C. for an additional 60 minutes. The mixture was diluted with EtOAc (50 mL) and washed with water (2×25 mL). The organic layer was dried over anhydrous Na2SO4, filtered and concentrated by rotary evaporation to yield the title compound (500 mg), which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09162982B2
Source datasetuspto-grants-2015_10
ORD IDord-cfec62ab06364c2994b8ee833bc0bfde
Source noteuspto-grants-2015_10