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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560941Generated: October 30, 2026

Acetone → 2-Fluoro-3-(hydroxymethyl)-6-iodobenzonitrile

https://huagongshe.com/reaction/560941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Fluoro-3-formyl-6-iodobenzonitrileHCID 86019349—
SolventMethanolHCID 887—
Product2-Fluoro-3-(hydroxymethyl)-6-iodobenzonitrileHCID 6668118963%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of Example 220A (5.0 g, 18 mmol) in MeOH (100 mL) at 0° C. was treated with NaBH4 (822 mg, 22 mmol) and the mixture was stirred for 1 h at 0° C. Acetone was added and the mixture was stirred for 5 min, then concentrated to dryness. The residue was partitioned between H2O and EtOAc. The extracts were washed with brine, dried (MgSO4) and concentrated. The residue was purified by flash chromatography on silica gel, eluting with 3:2 hexanes/EtOAc to give the desired product (3.14 g). Rf=0.38 (3:2 hexane:EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063091B2
Source datasetuspto-grants-2011_11
ORD IDord-5619aea17d144f378da2454f00c000ea
Source noteuspto-grants-2011_11