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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714813Generated: October 29, 2026

Water → HCID 67369163, compound

https://huagongshe.com/reaction/1714813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,6-LutidineHCID 7937—
ReactantTriisopropylsilyl trifluoromethanesulfonateHCID 2724529—
ReactantHCID 68576424HCID 68576424—
SolventDichloromethaneHCID 6344—
ProductHCID 67369163HCID 67369163—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 14.70 g of 4-(4-benzyloxyphenyl)-1-(1-phenylethyl)-1,2,3,4-tetrahydro-pyridin-3-ol [257928-45-3] in 250 ml of dichloromethane is mixed with 6.80 ml of 2,6-lutidine and cooled to 0° C. 12.60 ml of triisopropysilyl trifluoromethanesulphonate are added dropwise, and the reaction mixture is stirred at 0° C. for 1 hour. The reaction solution is poured into 400 ml of water, and the phases are separated. The aqueous phase is back-extracted with 200 ml of dichloromethane, and the combined organic phases are dried with sodium sulphate and evaporated. The title compound is obtained as a yellow-brown oil from the residue by flash chromatography (SiO2 F60). Rf (EtOAc/heptane 1:2)=0.66; Rt=5.83.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799779B2
Source datasetuspto-grants-2010_09
ORD IDord-2bc87c4a7502496991689e7f2efdaaec
Source noteuspto-grants-2010_09