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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272657Generated: October 26, 2026

Sodium Cyanide → 1-(3-Bromo-4-fluorophenyl)-1-cyanomethanol

https://huagongshe.com/reaction/272657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
Reactant3-Bromo-4-fluorobenzaldehydeHCID 173604—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product1-(3-Bromo-4-fluorophenyl)-1-cyanomethanolHCID 4343661692%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of sodium bisulfite (28.3 g, 271 mmol) in water at 50° C. is treated with 3-bromo-4-fluorobenzaldehyde (45.8 g, 225 mmol), stirred at 50° C. for 2 h, cooled with an ice bath, diluted with ether, treated dropwise with an aqueous solution of sodium cyanide (12.2 g, 248 mmol) over a period of 30 min and stirred at room temperature overnight. The reaction mixture is separated, and the aqueous phase is extracted with ether. The extracts are combined with the organic phase, washed with brine, dried over magnesium sulfate and concentrated to dryness to afford the title compound as a clear oil, 47.6 g (92% yield), identified by NMR analysis. 1H NMR (300 MHz, CDCl3) δ 7.75 (m, 1H), 7.47 (m, 1H), 7.23 (m, 1H), 5.54 (m, 1H), 3.19 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456186B2
Source datasetuspto-grants-2008_11
ORD IDord-6d1b69fd37f049abab1d5c9a36b457bc
Source noteuspto-grants-2008_11