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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3960Generated: October 24, 2026

Phenyl P,P-diphenylphosphinate → Sodium diphenylphosphinate

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Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl P,P-diphenylphosphinateHCID 15566—
ReactantSodium trimethylsilanolateHCID 23672319—
SolventTetrahydrofuranHCID 8028—
ProductSodium diphenylphosphinateHCID 2368056468%

Reaction Steps

The procedure of Example 1 was followed except that a mixture of phenyl diphenylphosphinate (13.76 g, 46.7 mmol), sodium trimethylsilanolate (5.6 g, 50 mmol), and dry tetrahydrofuran (175 mL) was left standing overnight (as it became impossible to stir). Sodium diphenylphosphinate (7.6 g, 68% yield) was isolated as a white solid: 1H NMR (D2O) δ 6.6-8.0 (m, Ar--H's 10H). Anal. Calcd. for C12H10NaO2P: C, 60.01; H, 4.20; P, 12.90. Found: C, 55.25, 55.47; H, 4.22, 4.20; P, 11.06, 11.15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04723016
Source datasetuspto-grants-1988_02
ORD IDord-ce46e031884641d0ad46ce0b09b270af
Source noteuspto-grants-1988_02