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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169698Generated: November 4, 2026

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

https://huagongshe.com/reaction/1169698

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2,6-Dichloro-3-fluorophenyl)ethanoneHCID 2733982—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product1-(2,6-Dichloro-3-fluorophenyl)ethan-1-olHCID 1677006888%

Reaction Steps

Sodium borohydride (90 mg, 2.4 mmol) was added to a solution of 2′,6′-dichloro-3′-fluoro-acetophenone (Aldrich, catalog #52, 294-5) (207 mg, 1 mmol) in 2 mL of anhydrous CH3OH. The reaction mixture was stirred at room temperature for 1 h then was evaporated to give a colorless oil residue. The residue was purified by flash chromatography (eluting with 0→10% EtOAc in hexanes) to give compound A1 as a colorless oil (180 mg; 0.88 mmol; 86.5% yield); MS (APCI) (M-H)− 208; 1H NMR (400 MHz, chloroform-D) δ ppm 1.64 (d, J=6.82 Hz, 3H) 3.02 (d, J=9.85 Hz, 1H) 6.97-7.07 (m, 1H) 7.19-7.33 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825137B2
Source datasetuspto-grants-2010_11
ORD IDord-856a06f20e9342f28c35d5736b2842ed
Source noteuspto-grants-2010_11