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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561961Generated: November 2, 2026

Ammonium Chloride → 1-(2-Fluoro-4-iodo-phenyl)-ethanol

https://huagongshe.com/reaction/561961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Fluoro-4-iodobenzaldehydeHCID 4090083—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1-(2-Fluoro-4-iodo-phenyl)-ethanolHCID 5341545384%

Reaction Steps

To a solution of 2-fluoro-4-iodo-benzaldehyde (17.40 g, 69.60 mmol) in anhydrous tetrahydrofuran (300 mL) at −10° C. under an atmosphere of nitrogen was added 3.0 M methylmagnesium chloride in tetrahydrofuran (27.84 mL, 83.52 mmol) via syringe at such a rate as to maintain the temperature of the reaction mixture below 0° C. The reaction was stirred for 30 minutes while warming to room temperature. Saturated aqueous ammonium chloride solution was added and the mixture was diluted with ethyl acetate (200 mL). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (2×50 mL). The organic extracts were combined, washed with water (1×50 mL), brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by chromatography over silica gel gradient eluted with 15 to 40% v/v ethyl acetate/hexanes to give 1-(2-fluoro-4-iodo-phenyl)-ethanol (15.50 g, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063085B2
Source datasetuspto-grants-2011_11
ORD IDord-09bce76d8f3446c5acdd340bb3174881
Source noteuspto-grants-2011_11