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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275656Generated: October 29, 2026

Methanol → ethyl N-(4-chloro-6-fluoro-2-methoxy-3-nitrophenyl)carbamate

https://huagongshe.com/reaction/275656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactantethyl N-(4-chloro-2,6-difluoro-3-nitrophenyl)carbamateHCID 18315089—
Solvent1,4-DioxaneHCID 31275—
Productethyl N-(4-chloro-6-fluoro-2-methoxy-3-nitrophenyl)carbamateHCID 1831506066.8%

Reaction Conditions

Temperature65 °C

Reaction Steps

Under a nitrogen atmosphere, a solution of 30.6 grams (0.109 mole) of ethyl N-(4-chloro-2,6-difluoro-3-nitrophenyl)carbamate and 18 mL (0.449 mole) of methanol in 175 mL of dioxane was stirred and 218 mL (0.218 mole) of 1M sodium trimethylsilanoate (in tetrahydrofuran) was added dropwise during a 45 minute period. Upon completion of addition, the reaction mixture was heated to 65° C. where it stirred for three hours. At the conclusion of this period, the reaction mixture was allowed to cool to ambient temperature where it stirred for about 18 hours. The reaction mixture was concentrated under reduced pressure to a residue. The residue was taken up in cold 3N hydrochloric acid. The resulting solid was collected by filtration, washed with petroleum ether, and heat dried under vacuum, yielding 21.3 grams of title compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352958B1
Source datasetuspto-grants-2002_03
ORD IDord-2d93098cff934c5ba43795fef1435a25
Source noteuspto-grants-2002_03