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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251031Generated: November 3, 2026

Sodium Methoxide → o-Phenylbenzoic acid

https://huagongshe.com/reaction/1251031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 10967324HCID 10967324—
ReactantHCID 11043594HCID 11043594—
SolventMethanolHCID 887—
Producto-Phenylbenzoic acidHCID 7035753.8%
ProductEthyl 2-phenylbenzoateHCID 992095223.7%

Reaction Steps

To a stirred solution of a mixture(620 mg, 2.54 mmol) of ethyl 4-chloro-2-phenylcyclohexa-2,4-dienecarboxylate and ethyl 4-chloro-2-phenylcyclohexa-1,3-dienecarboxylate in MeOH(5 ml), NaOMe(28% in MeOH, 1.98 g, 10.1 mmol) was added. After stirring for 17 hr at room temperature, the solvent was evaporated under reduced pressure. Water was added to the residue and dil. HCl aq., and it was extracted with AcOEt. The organic layer was washed with brine and dried over MgSO4. After removal of the solvent, the residue was purified by column chromatography on silica gel with n-hexane-AcOEt to afford 136 mg of ethyl 2-phenylbenzoate(y=23.7%) and 236 mg of 2-phenylbenzoic acid(y=53.8%). 1H-NMR(ppm, 300 MHz, CDCl3) δ ester 7.82(1H, dd, J=1.4 and 7.7 Hz), 7.10-7.60(8H), 4.08(2H, d, J=7.0 Hz), 0.98(3H, t, J=7.0 Hz); acid 7.95(1H, d, J=7.9 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340772B1
Source datasetuspto-grants-2002_01
ORD IDord-ff111a659b9b44959a78918df1ff6e7d
Source noteuspto-grants-2002_01