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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931885Generated: October 31, 2026

Methyl 4-chlorobenzoate → HCID 58573710, compound

https://huagongshe.com/reaction/931885

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

To a solution of 2-(3-chlorophenyl)acetic acid (10 g, 58.6 mmol) in THF (58 ml) was added 117 mL of a 1M solution of sodium bis-(trimethylsilyl) amide in THF slowly over 1 h at −78° C. After being stirred at −78° C. for 40 min, a solution of methyl 4-chlorobenzoate (10 g, 58.6 mmol) in THF (35 ml) was added over a period of 10 min. The reaction was stirred at −78° C. for 3 h, then allowed to warm to 25° C., and stirred an additional 2 h until completion. The reaction was quenched with saturated aqueous NH4Cl solution and most of the THF was removed under reduced pressure. The residue was extracted with ethyl acetate (2×100 ml). The combined organic layers were washed with sat. NaCl solution, dried over Na2SO4, 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 numberUS09296736B2
Source datasetuspto-grants-2016_03
ORD IDord-cedeb2728a3d487781a5275f22e81ec4
Source noteuspto-grants-2016_03