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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337583Generated: October 30, 2026

Methanol → (5-Bromo-2,3-dichlorophenyl)methanol

https://huagongshe.com/reaction/337583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
Reactant5-Bromo-2,3-dichlorobenzaldehydeHCID 77231202—
SolventTetrahydrofuranHCID 8028—
Product(5-Bromo-2,3-dichlorophenyl)methanolHCID 66896066—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 5:1 (v/v) MeOH:THF solution (0.38 M) of 5-bromo-2,3-dichlorobenzaldehyde (1 eq.) from Step 1, Amine 5 was added at 0° C. sodium borohydride (1.1 eq.) portionwise over 45 min. The reaction solution was stirred at 0° C. for 2 h before the volatiles were removed in vacuo. The resulting residue was then partitioned between ether and 10% aq. HCl. The aqueous layer was separated and back-extracted with ether. The combined organic extracts were washed further with 1 N aq. NaOH, water and brine, dried Na2SO4, filtered and the filtrate concentrated in vacuo. Purification of the crude product thus obtained by way of flash chromatography (SiO2, 9:1 (v/v) Hex:EtOAc→3:7 (v/v) Hex:EtOAc) afforded the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889714B2
Source datasetuspto-grants-2014_11
ORD IDord-f3f42687c21b4a409166931e6db466ee
Source noteuspto-grants-2014_11