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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290642Generated: October 27, 2026

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

https://huagongshe.com/reaction/1290642

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 (109 mmole) of ethyl N-(4-chloro-2,6-difluoro-3-nitrophenyl)carbamate and 18 mL (449 mmole) of methanol in 175 mL of dioxane was stirred, and 218 mL (218 mmole) of 1M sodium trimethylsilanoate (in tetrahydrofuran) was added dropwise during a 45 minute period. Upon completion of the 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, which 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 ethyl N-(4-chloro-6-fluoro-2-methoxy-3-nitrophenyl)carbamate. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753595
Source datasetuspto-grants-1998_05
ORD IDord-89fbab9247dd444f98b64809e6f2b95a
Source noteuspto-grants-1998_05