HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973648Generated: October 27, 2026
Water → Ethyl diethoxymethyl(benzyl)phosphinate
https://huagongshe.com/reaction/973648
Participants
| Role | Name | HCID | Charge |
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| 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 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 extracted 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). 'H-NMR (CDCl3): δ (ppm)=7.29 (5 H, m, Ph), 4.48 (1 H d, 5=9 HZ, CHP), 4.08 (2 H, q, CH2OP), 3.83 (2 H, m, CH2OC), 3.66 (2 H, m, CH2OC), 3.21 (2 H, ABq, d, 5=15×6 HZ, CH2P), 1,23 (9 H, m, 3×CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05064819 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-8b93364b91594bffacc43ad90dd1759e |
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| Source note | uspto-grants-1991_11 |
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