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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3943Generated: October 25, 2026

Phenyl benzoate → Potassium Benzoate

https://huagongshe.com/reaction/3943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl benzoateHCID 7169—
ReactantPotassium trimethylsilanolateHCID 23668039—
SolventTetrahydrofuranHCID 8028—
ProductPotassium BenzoateHCID 2366196074%

Reaction Steps

The procedure of Example 1 was followed using phenyl benzoate (3.96 g, 20 mmol), potassium trimethylsilanolate (2.56 g, 20 mmol), dry tetrahydrofuran (50 mL), and a 5 h reaction time. Potassium benzoate (2.37 g, 74% yield) was isolated as a white solid: 1H NMR (D2O, DSS, 80 MHz) δ 7.4-8.0 (m, Ar--H's, 5H). Anal. Calcd. for C7H5KO2 : C, 52.48; H, 3.15; K, 24.41, Found: C, 50.28, 50.15, 52.45; H, 3.28, 3.36, 3.24; K, 24.80.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04723016
Source datasetuspto-grants-1988_02
ORD IDord-246351cf446448bb94fc9b6d5752a45c
Source noteuspto-grants-1988_02