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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096822Generated: October 25, 2026

Methanol → Benzenemethanol, 3,5-dichloro-4-hydroxy-

https://huagongshe.com/reaction/1096822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
Reactant3,5-Dichloro-4-hydroxybenzoic acidHCID 18749—
SolventTetrahydrofuranHCID 8028—
ProductBenzenemethanol, 3,5-dichloro-4-hydroxy-HCID 176409—

Reaction Conditions

Temperature0 °C

Reaction Steps

BH3 (1M in THF, 250 mL, 250 mmol) was added dropwise to a cooled sol. of 3,5-dichloro-4-hydroxybenzoic acid (20 g, 96.6 mmol) in THF (200 mL) at 0° C. The resulting mixture was stirred at 0° C. for 15 min., and then at rt for 13 h. The milky mixture was cooled to 0° C., and MeOH (150 mL), then water (100 mL), were added dropwise. The mixture was further stirred at 0° C. for 15 min, and then at rt for 5 h. The mixture was then partially concentrated under reduced pressure. EtOAc (200 mL) and water (50 mL) were added to the residue, and the phases were shaken and separated. The aq. phase was further extracted with EtOAc. The combined org. extracts were washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure. Purification by FC(CH2Cl2/CH3OH, 100:1) led to the title compound as a slightly beige solid (17.86 g, 96%). LC-MS: tR=0.69 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138340B2
Source datasetuspto-grants-2012_03
ORD IDord-90e996b781944c7a9eb2dd649fbe0bcb
Source noteuspto-grants-2012_03