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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207127Generated: November 2, 2026

Methyl 4-chlorobenzoate → HCID 58573710, compound

https://huagongshe.com/reaction/2207127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-chlorobenzoateHCID 14307—
Reactant3-Chlorophenylacetic acidHCID 15879—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58573710HCID 58573710—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Sodium bis(trimethylsilyl)amide (1 M in tetrahydrofuran, 117 mL) was slowly added to a −78° C. solution of 2-(3-chlorophenyl)acetic acid (10 g, 58.6 mmol) in tetrahydrofuran (58 mL) over 1 hour. After stirring at −78° C. for 40 minutes, a solution of methyl 4-chlorobenzoate (10 g, 58.6 mmol) in tetrahydrofuran (35 mL) was added over a period of 10 minutes. The reaction was stirred at −78° C. for 3 hours then allowed to warm to 25° C. After two hours at 25° C., the reaction was quenched with saturated aqueous ammonium chloride solution, and most of the tetrahydrofuran was removed under reduced pressure. The residue was extracted with ethyl acetate (2×100 mL). The combined organic layers were washed with saturated sodium chloride solution, dried over sodium sulfate, filtered and the filtrate was concentrated. The product was recrystallized from ether/pentane to provide the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376386B2
Source datasetuspto-grants-2016_06
ORD IDord-ca2352e930494ae3b3ab85ba219d53b0
Source noteuspto-grants-2016_06