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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372996Generated: October 25, 2026

Boron trifluoride etherate → 4-cyanophenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranoside

https://huagongshe.com/reaction/2372996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
Reactant4-CyanophenolHCID 13019—
ReactantSodium BicarbonateHCID 516892—
Reactant2,3,4-tri-O-acetyl-5-thio-alpha-D-xylopyranosyl trichloroacetimidateHCID 21631547—
SolventDichloromethaneHCID 6344—
Product4-cyanophenyl 2,3,4-tri-O-acetyl-5-thio-beta-D-xylopyranosideHCID 1506784680%

Reaction Steps

1 ml of a 0.1M solution of boron trifluoride etherate in methylene chloride is added at -15° C., under an inert atmosphere, to a suspension of 250 mg (0.57.10-3 mol) of 2,3,4-tri-O-acetyl-5-thio-α-D-xylopyranosyl trichloroacetimidate, 57 mg (0.48.10-3 mol) of 4-hydroxybenzonitrile and a molecular sieve (1 nm) in 10 ml of methylene chloride. The reaction medium is allowed to return gradually to 0° C. and, after a reaction time of 3 h, is neutralized with sodium bicarbonate. The reaction mixture is then washed with water and dried over magnesium sulfate, MgSO4, and the solvent is evaporated off under reduced pressure. 150 mg (yield: 80%) of the expected product are obtained after purification by chromatography on silica gel using a hexane/ethyl acetate mixture (2/1 v/v) as the eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05101048
Source datasetuspto-grants-1992_03
ORD IDord-7db8332caff147d482a7de8f5ef25b1e
Source noteuspto-grants-1992_03