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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867243Generated: October 30, 2026

Methanol → Methyl 2-chloro-4-t-butylbenzoate

https://huagongshe.com/reaction/1867243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant1,3-Bis(phenylphosphino)propaneHCID 4366891—
ReactantTrifluoro-methanesulfonic acid 4-tert-butyl-2-chloro-phenyl esterHCID 17859607—
Catalystpalladium(II) acetateHCID 167845—
SolventHCID 178418416HCID 178418416—
ProductMethyl 2-chloro-4-t-butylbenzoateHCID 17859604—

Reaction Steps

The triflate compound (638 mg, 2 mmol) obtained in Step 1-2, palladium acetate (14 mg), 1,3-diphenylphosphinopropane (25 mg), methanol (4 ml) and triethylamine (0.6 ml) were dissolved in dimethylformamide (5 ml), and the obtained solution was stirred at 80° C. in carbon monoxide atmosphere for 16 hours. After leaving the reaction mixture to cool followed by the extraction with ethyl acetate/hexane and the purification by the silica gel column chromatography, methyl 2-chloro-4-t-butylbenzoate was obtained. The ester thus obtained was dissolved in dichloromethane (2 ml). 1 M solution (2.5 ml) of diisobutylaluminum hydride in toluene was added dropwise to the obtained solution at −78° C. in argon atmosphere, and the resulting solution was stirred at that temperature for 5 minutes. 0.5 M hydrochloric acid (20 ml) was added to the reaction mixture, and the temperature was elevated to room temperature. After the extraction with ethyl acetate followed by the purification by the silica gel column chromatography, 2-chloro-4-t-butylbenzyl alcohol (yield: 204 mg, 51%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632830B2
Source datasetuspto-grants-2009_12
ORD IDord-18be6e67c21746b492c8c2f242f2c412
Source noteuspto-grants-2009_12