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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519280Generated: October 25, 2026

Sodium borohydride → (2,6-Dibromo-4-fluorophenyl)methanol

https://huagongshe.com/reaction/519280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2,6-Dibromo-4-fluorobenzaldehydeHCID 44474666—
SolventEthanolHCID 702—
Product(2,6-Dibromo-4-fluorophenyl)methanolHCID 5804394375%

Reaction Conditions

Temperature10 °C

Reaction Steps

To a solution of 104k (20 g, 71 mmol) in EtOH (500 mL) was added NaBH4 (10 g, 284 mmol). The mixture was stirred at room temperature (10° C.) for 4 h and TLC showed the starting material had disappeared. The reaction was quenched by aqueous HCl solution (150 mL, 1M) and evaporated in vacuo until most of EtOH was distilled. The residue was extracted by ethyl acetate (500 mL×3). The organic layers were combined, dried with Na2SO4, and evaporated in vacuo. The residue was purified by silica-gel column chromatography eluting with petroleum ether/ethyl acetate (from 50:1 to 20:1) to give 104l as a white solid (15g, 75%). MS: [M-OH]+ 267. 1H NMR (500 MHz, DMSO-d6) δ 7.68 (d, J=8.5, 2H), 5.23 (s, 1H), 4.71 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115152B2
Source datasetuspto-grants-2015_08
ORD IDord-ec5e5eb9257c4a00ae276016995db32f
Source noteuspto-grants-2015_08