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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1612784Generated: October 31, 2026

Boron trifluoride etherate → HCID 54257178, compound

https://huagongshe.com/reaction/1612784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantEthyl orthoformateHCID 31214—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178476801HCID 178476801—
ProductHCID 54257178HCID 54257178—

Reaction Steps

A solution of 1.68 g of ethyl 2-(4-chlorophenyl)prop-1-enylphosphinate in 20 ml of triethyl orthoformate is treated with 0.1 g of boron trifluoride diethyl etherate and the resulting solution stirred for 7 days at room temperature. The reaction mixture is then treated with 20 ml 10% aqueous sodium hydrogen carbonate solution and extracted twice with dichloromethane. The organic layer is removed, dried and concentrated to give an oil. Chromatography on silica gel gives ethyl 2-(4-chlorophenyl)prop-1-enyl-(diethoxymethyl)phosphinate as a colourless oil. 1H-NMR (CDCl3): δ(ppm)=7.38 (4H, m; Ph), 5.51 (1H, d, CH), 4.62 (1H, d, CH--P), 4.05 (2H, q, CH2OP), 3.88-3.56 (CH, m, 2×CH2OC), 2.07 (2H, d, d, CH2P), 1.28-1.14 (9H, m, 3×CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05190934
Source datasetuspto-grants-1993_03
ORD IDord-553b22b701154d608d1174671f1b5804
Source noteuspto-grants-1993_03