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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006839Generated: October 29, 2026

Trifluoromethanesulfonic acid → HCID 22671865, compound

https://huagongshe.com/reaction/1006839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantBenzyl 2,2,2-trichloroacetimidateHCID 144968—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22671871HCID 22671871—
SolventDichloromethaneHCID 6344—
SolventCyclohexaneHCID 8078—
ProductHCID 22671865HCID 2267186597.2%

Reaction Steps

(6-ring): To a solution of (2RS,5RS)-(5-tert-butoxymethyl-1-methanesulfonyl-piperidin-2-yl)-methanol (2.80 g) in dichloromethane (20 ml) and cyclohexane (30 ml) was added benzyl 2,2,2-trichloroacetimidate (3.03 g) and trifluoromethanesulphonic acid (0.2 ml). The reaction mixture was stirred 1 h at room temperature, poured onto a saturated sodium bicarbonate solution and extracted with EtOAc. The organic phase was washed with brine, dried over magnesium sulphate and concentrated. The residue was chromatographed on silica gel using EtOAc/hexane 1:3 and 1:2 as eluents to obtain (2RS,5RS)-2-benzyloxymethyl-5-tert-butoxymethyl-1-methanesulfonyl-piperidine (3,6 g) as a syrup, MS: 369 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06790860B2
Source datasetuspto-grants-2004_09
ORD IDord-d43cfdd134164960b11ec6434c9afdbb
Source noteuspto-grants-2004_09