HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483993Generated: October 27, 2026
Water → Ethyl diethoxymethyl(benzyl)phosphinate
https://huagongshe.com/reaction/483993
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178472284 | HCID 178472284 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl diethoxymethyl(benzyl)phosphinate | HCID 9994134 | — |
Reaction Steps
A solution of diethoxymethylphosphinic acid ethyl ester is added within a period of 90 minutes, under argon, to a suspension of 13.2 g of 99% sodium hydride in 500 ml of tetrahydrofuran, the temperature being maintained at 20°. The reaction is exothermic and is accompanied by the evolution of gas. The mixture is then stirred for 90 minutes, and 85.5 g of benzyl bromide are then added within a period of 20 minutes. The mixture is then stirred at room temperature for 24 hours and cooled to 0°, and 100 ml of water are added carefully. The organic solvents are removed under reduced pressure and the residue is partitioned between water and dichloromethane. The organic phase is separated off, washed with water, dried over sodium sulfate and concentrated by evaporation. Distillation of the residue under reduced pressure yields diethoxymethyl(benzyl)phosphinic acid ethyl ester having a boiling point of 103°-110° (3×10-4 bar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05229379 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-0d3307dbc4a943608820676465e53bde |
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| Source note | uspto-grants-1993_07 |
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