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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374465Generated: October 30, 2026

1,3-Difluoro-2-(methoxymethoxy)-5-nitrobenzene → HCID 68615412, compound

https://huagongshe.com/reaction/2374465

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Difluoro-2-(methoxymethoxy)-5-nitrobenzeneHCID 68615889—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 68615412HCID 68615412—

Reaction Steps

A suspension of 3,5-difluoro-4-(methoxymethyl)oxynitrobenzene (35.0 g) and palladium catalyst (10% on charcoal, 3.00 g) in methanol (250 mL) ) was hydrogenated at 1 atm for 2 hours at room temperature. After filtration of the catalyst, the filtrate was concentrated in vacuo to give 4-amino-2,6-difluoro-1-(methoxymethyl)oxybenzene. This was used in the next step without further purification. To a solution of crude 4-amino-2,6-difluoro-1-(methoxymethyl)oxybenzene thus obtained in tetrahydrofuran (500 mL) was successively added sodium hydrogencarbonate (17.4 g), water (100 mL) and benzyl chloroformate (30.0 g) at 0° C., and the mixture was stirred at room temperature for 15 minutes. The mixture was diluted with saturated sodium hydrogencarbonate solution and extracted with ethyl acetate. The organic extracts were washed with brine, dried over anhydrous magnesium sulfate, and then concentrated in vacuo. Flash chromatography (silica, hexane:ethyl acetate=6:1) of the residue gave Reference Example 8 (49.10 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462633B2
Source datasetuspto-grants-2008_12
ORD IDord-dbd54c19d9e240e588f73592fd8efa8c
Source noteuspto-grants-2008_12