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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875412Generated: October 26, 2026

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

https://huagongshe.com/reaction/875412

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 numberUS08980911B2
Source datasetuspto-grants-2015_03
ORD IDord-6dc1f2d7982d47929c08e708e487565d
Source noteuspto-grants-2015_03