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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399557Generated: October 31, 2026

Boron trifluoride etherate → HCID 22856009, compound

https://huagongshe.com/reaction/2399557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantTrimethylsilyl cyanideHCID 82115—
ReactantHCID 54468030HCID 54468030—
SolventNitromethaneHCID 6375—
ProductHCID 22856009HCID 2285600971%

Reaction Steps

To a stirred solution of 2,4-di-O-benzyl-3-O-methyl-a,b-D-xylopyranosyl acetate (20 g, 0.052 mole) and Me3SiCN (20 ml, 0.16 mole) in anhydrous nitromethane (300 ml) was added boron trifluoride etherate (1.0 g, 0.007 mole) at room temperature. After the mixture was stirred at room temperature for 30 min, the mixture was evaporated to dryness under reduced pressure. The residue was chromatographed on silica gel using CH2Cl2 /AcOEt (99:1) as an eluent to give 2,4-di-O-benzyl-3-O-methyl-a,b-D-xylopyranosyl cyanide as colorless oil (13.0 g, 71% yield); EI-MS: m/z 353 (M+), 262 (M+ -Bn); 1H-NMR of b-cyano-isomer (CDCl3)d; 3.15 (1H,dd,J=10,11 Hz), 3.23 (1H,t,J=10 Hz), 3.49 (1H,m), 3.59 (1H,t,J=10 Hz), 3.66 (3H,s), 3.96 (1H,dd,J=5 & 11 Hz), 3.97 (1 H,d,J=10 Hz), 4.61 (1H,d,J=12 Hz),4.73 (1H,d,J=12 Hz), 4.84 (1H,d,J=11 Hz), 4.88 (1H,d,J=11 Hz), 7.29~7.42 (10H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05449785
Source datasetuspto-grants-1995_09
ORD IDord-f6ddb3321525483cbf9f6acc1ae490e5
Source noteuspto-grants-1995_09