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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968982Generated: October 29, 2026

1,4-Dioxane → 4-(Difluoromethoxy)-2-aminophenol

https://huagongshe.com/reaction/1968982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant4-(Difluoromethoxy)-2-nitrophenolHCID 59444071—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventWaterHCID 962—
Product4-(Difluoromethoxy)-2-aminophenolHCID 5944413157.9%

Reaction Steps

A mixture of 4-(difluoromethoxy)-2-nitrophenol (D94, 450 mg, 1.974 mmol), Raney-nickel (est. 200 mg), 1,4-dioxane (10 mL) and water (5 mL) was stirred at room temperature in a hydrogen atmosphere for 20 h. The reaction mixture was filtered through kieselguhr under an argon atmosphere and evaporated to dryness. The unreacted starting material was sufficiently volatile that most of it was removed by using a rotary evaporator. The residue was purified by flash column chromatography on a pre-packed silica cartridge (column size 50 g), eluting with 0-30% ethyl acetate in hexane, followed by 10-50% 2 M ammonia in methanol in DCM. The residue was further purified on an IST SCX-2 cartridge 20 g, washing with methanol (125 mL) and eluting with 2 M ammonia in methanol (125 mL). The basic eluent was evaporated to dryness to afford the desired product (D95) as a brown solid (200 mg). (M+H)+=176.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426443B2
Source datasetuspto-grants-2013_04
ORD IDord-24401b508fb746859bec2a86ace7d999
Source noteuspto-grants-2013_04