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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499579Generated: November 1, 2026

3,5-Difluorobenzaldehyde → 3,5-Difluorobenzyl alcohol

https://huagongshe.com/reaction/1499579

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-DifluorobenzaldehydeHCID 588160—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product3,5-Difluorobenzyl alcoholHCID 522721—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a solution of 3,5-difluorobenzaldehyde (2.00 g, 14.1 mmol) in MeOH (20 mL) at 0-5° C. was added NaBH4 (1.06 g, 28.1 mmol) portionwise. The mixture was stirred at 0-5° C. for 1 h, quenched with brine, and then extracted with EtOAc (2×). The combined organic phases were washed with water and brine, then dried over Na2SO4 and concentrated under reduced pressure to give sub-title compound as a colorless oil. %). 1H NMR (300 MHz, CDCl3) δ 6.88 (m, 2H), 6.70 (m, 1H), 4.69 (s, 2H), 1.88 (br s, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09200004B2
Source datasetuspto-grants-2015_12
ORD IDord-1e8cd699dd444c3db7e420ab3ce7a7a5
Source noteuspto-grants-2015_12