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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463643Generated: October 27, 2026

Water → Ethyl diethoxymethyl(benzyl)phosphinate

https://huagongshe.com/reaction/1463643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178472284HCID 178472284—
SolventTetrahydrofuranHCID 8028—
ProductEthyl diethoxymethyl(benzyl)phosphinateHCID 9994134—

Reaction Steps

A suspension of 12 g of oil-free sodium hydride in 300 ml of absoluted tetrahydrofuran under an inert atmosphere is treated with a solution of 103.5 g of 95% ethyl diethoxymethylphosphinate in 100 ml of absolute tetrahydrofuran at such a rate so as to maintain the temperature at or just below 20° C. After the addition is complete, the suspension is stirred for 1 hour at room temperature and then cooled to approximately 10° C. before addition of 85.5 g of benzylbromide, maintaining the temperature below 15° C. Finally, the white suspension is stirred for 20 hours at room temperature. Water is then added and the tetrahydrofuran layer is separated. The aqueous layer is extractet with dichloromethane and the combined organic layers are dried and concentrated in vacuo. Distillation of the residue in high vacuum affords ethyl diethoxymethyl(benzyl)phosphinate as a colourless oil of b.p. 105-125 (10-2 mbar). 1H-NMR (CDCl3): δ (ppm)=7.29 (5H, m, Ph), 4.48 (1H, d, 5=9 Hz, CHP), 4.08 (2H, q, CH2OP), 3.83 (2H, m, CH2OC), 3.66 (2H, m, CH2OC), 3.21 (2H, ABq, d, 5=15×6 Hz, CH2P), 1.23 (9H, m, 3×CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05300679
Source datasetuspto-grants-1994_04
ORD IDord-e1585ef08c884a5e8dd7246d50347a74
Source noteuspto-grants-1994_04