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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587106Generated: October 26, 2026

Ammonium Chloride → 1-(2,6-Dichloro-3-fluorophenyl)ethan-1-ol

https://huagongshe.com/reaction/587106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(2,6-Dichloro-3-fluorophenyl)ethanoneHCID 2733982—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product1-(2,6-Dichloro-3-fluorophenyl)ethan-1-olHCID 16770068105.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2′,6′-dichloro-5′-fluoroacetophenone (10.4 g, 50 mmol) in MeOH (anhydrous, 80 mL) was added NaBH4 (3.78 g, 100 mmol) in portions at 0° C. After the addition of NaBH4, the solution was stirred at 0° C. for 10 min, then allowed to warm to room temperature and stirred at room temperature for 30 min. The reaction solution was concentrated to remove the solvent to give the residue. A saturated solution of NH4Cl (60 mL) was added slowly. The aqueous phase was then extracted with EtOAc (3×65 mL). The combined organic phase was washed with H2O (50 mL) and brine (50 mL), dried over anhydrous Na2SO4, concentrated by evaporation in vacuo to afford (±)1-(2,6-dichloro-3-fluorophenyl)ethanol (11 g, 100%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226923B2
Source datasetuspto-grants-2016_01
ORD IDord-b209ca1998d24726b377f015c5e648c6
Source noteuspto-grants-2016_01