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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256221Generated: October 30, 2026

Triethylamine → 1,1-Dimethylethyl (1-trifluoromethanesulphonylpiperidin-4-yl)carbamate

https://huagongshe.com/reaction/1256221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoromethanesulfonyl chlorideHCID 79000—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product1,1-Dimethylethyl (1-trifluoromethanesulphonylpiperidin-4-yl)carbamateHCID 86664928—

Reaction Conditions

Temperature0 °C

Reaction Steps

A 150 ml round-bottomed flask equipped with a magnetic stirrer is charged under argon with 2 g of 4-N-boc-aminopiperidine in 35 ml of DCM, 82 mg of 4-dimethylaminopyridine (DMAP) and 1.86 ml of triethylamine. After cooling to 0° C. using an ice bath, 1.6 ml of trifluoromethanesulphonyl chloride are added dropwise. The mixture is stirred at 0° C. for 30 min and then at RT for 1 h. It is poured into 100 ml of saturated aqueous sodium bicarbonate solution. It is extracted with AcOEt, washed with saturated aqueous NaCl solution, dried over MgSO4, filtered and concentrated to dryness under RP. Chromatography on silica gel (15-40 μm), eluting with a mixture of DCM and methanol (98/02 by vol.), gives 1.5 g of 1,1-dimethylethyl (1-trifluoromethanesulphonylpiperidin-4-yl)carbamate (cream solid). MS (E/I): m/z=232 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461175B2
Source datasetuspto-grants-2013_06
ORD IDord-55bd18416942432db94e68621e464505
Source noteuspto-grants-2013_06