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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392494Generated: October 30, 2026

Triethylamine → Tert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/392494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(methylsulfonyloxymethyl)piperidine-1-carboxylateHCID 2765838—

Reaction Conditions

Temperature0 °C

Reaction Steps

The title compound from Step A above (8.8 g, 40.87 mmoles) and triethylamine (8.55 mL, 61.31 mmoles) were dissolved in CH2Cl2 (100 mL) and the mixture was stirred under nitrogen at 0° C. Methanesulfonylchloride (3.8 mL mL, 49.05 mmoles) was added and the solution was stirred at room temperature for 2 h. The solution was diluted with CH2Cl2 and washed with saturated aqueous sodium bicarbonate, water and dried (MgSO4), filtered and evaporated to dryness to give the title compound (12.8 g) FABMS (M+1)=294.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800636B2
Source datasetuspto-grants-2004_10
ORD IDord-7f078268d62e4e8490d587af3b058b97
Source noteuspto-grants-2004_10