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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861956Generated: November 2, 2026

Trimethyl borate → (2-Methoxy-3-nitrophenyl)methanol

https://huagongshe.com/reaction/1861956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl borateHCID 8470—
ReactantMethyl 2-methoxy-3-nitrobenzoateHCID 590805—
ReactantLithium borohydrideHCID 4148881—
SolventTetrahydrofuranHCID 8028—
Product(2-Methoxy-3-nitrophenyl)methanolHCID 1878967976.1%

Reaction Steps

A mixture of 2-methoxy-3-nitrobenzoic acid methyl ester (4.82 g), lithium borohydride (298 mg), trimethyl borate (0.27 ml) and anhydrous tetrahydrofuran (200 ml) was heated under reflux for 5 h. The reaction mixture was distilled under reduced pressure and ethyl acetate and water were added to the resulting residue. The organic layer was washed with a saturated aqueous sodium chloride solution, dried with anhydrous sodium sulfate and distilled under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent, n-hexane:ethyl acetate=1:1) to give 3.18 g of the titled compound (yield, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06534546B1
Source datasetuspto-grants-2003_03
ORD IDord-b7f432aefc3d4a9da316f54fa294f86b
Source noteuspto-grants-2003_03