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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1055422Generated: October 29, 2026

2-(DIFLUOROMETHOXY)-1-NAPHTHALDEHYDE → [2-(Difluoromethoxy)naphthalen-1-yl]methanol

https://huagongshe.com/reaction/1055422

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(DIFLUOROMETHOXY)-1-NAPHTHALDEHYDEHCID 818166—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product[2-(Difluoromethoxy)naphthalen-1-yl]methanolHCID 4339458139%

Reaction Steps

NaBH4 (255 mg, 6.73 mmol) was added to a suspension of 2-(difluoromethoxy)-1-naphthaldehyde (0.997 g, 4.49 mmol) in EtOH (29.9 mL). After 3 h the mixture was diluted with H2O, extracted with EtOAc, the combined extracts were washed with brine (200 mL), dried over Na2SO4, filtered, and the filtrate concentrated to give a residue that was purified by silica gel chromatography to provide (2-(difluoromethoxy)naphthalen-1-yl)methanol (387 mg, 39%) as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394263B2
Source datasetuspto-grants-2016_07
ORD IDord-331b8d17532b4ac585ee90dc9feafdcb
Source noteuspto-grants-2016_07