Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201805Generated: October 25, 2026

Methanol → Methyl 2,6-dichloro-4-(hydroxymethyl)benzoate

https://huagongshe.com/reaction/2201805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantDimethyl 2,6-dichloroterephthalateHCID 7730227—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2,6-dichloro-4-(hydroxymethyl)benzoateHCID 6671292080%

Reaction Steps

A solution of dimethyl 2,6-dichlorobenzene-1,4-dicarboxylate (2.3 g, 8.7 mmol) in tetrahydrofuran (10 mL) was treated with sodium borohydride (0.496 g, 13 mmol) and heated to refluxing temperature. The reaction mixture was then treated drop wise with methanol (1 mL) and continued refluxing for about 2 hours. The reaction mixture was warmed to room temperature and quenched with saturated aqueous ammonium chloride solution followed by partitioning with ethyl acetate. The combined organic layer was washed with brine, dried over sodium sulfate, filtered and concentrated. The crude product was purified by silica gel column chromatography using ethyl acetate in hexane (10%) as an eluant to yield methyl 2,6-dichloro-4-(hydroxymethyl)benzoate as a colorless liquid (1.6 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364466B2
Source datasetuspto-grants-2016_06
ORD IDord-0a80337fcf494295834c2681c507fd2a
Source noteuspto-grants-2016_06