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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488278Generated: November 5, 2026

Boron trifluoride etherate → HCID 131736871, compound

https://huagongshe.com/reaction/1488278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantTriethylamineHCID 8471—
Reactantbenzyl N-(2-hydroxyethyl)carbamateHCID 280458—
ReactantHCID 11012995HCID 11012995—
Solvent2-OxopropiononitrileHCID 69430—
ProductHCID 131736871HCID 131736871—

Reaction Steps

To a stirred solution of 1,2,3,4-tetra-O-acetyl-L-fucopyranose (200 g, 601.86 mmol) in AcCN (100 mL) and benzyl (2-hydroxyethyl)carbamate (140.96 g, 722.08 mmol) at 0° C. was added BF3.Et2O (427.7 g, 3.01 mol) dropwise over 2 hr. After stirring at rt for 16 hr, the reaction mixture was cooled to 0° C. and followed by the addition of Et3N (130 mL). The resulting mixture was concentrated and the residual was dissolved in CH2Cl2 (2.0 L), which was subsequently washed with sat. NaHCO3 (2×500 mL), water (2×500 mL) and brine (500 mL). The organic phase was separated, dried over Na2SO4, and concentrated. The residue was purified by flash chromatography on silica gel, eluting with EtOAc/petroleum ether (1:3) to give the title compound. 1H NMR (CDCl3) δ 7.33-7.37(5H, m), 5.12-5.32(5H, m), 4.99-5.04(1H, m), 4.42-4.45 (1H, d), 3.87-3.94 (1H, m), 3.78-3.84 (1H, m), 3.66-3.70(1H, m), 3.42-3.44 (2H, m), 2.19 (3H, s), 2.05-2.12(6H, m), 1.25-1.30 (3H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09427475B2
Source datasetuspto-grants-2016_08
ORD IDord-7fd683512bcb4a30a520ca0c29de644a
Source noteuspto-grants-2016_08