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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704468Generated: October 25, 2026

Dimethylformamide → 4-Chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)nitrobenzene

https://huagongshe.com/reaction/704468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantAcetic acid, chloro-, pentyl esterHCID 138488—
ReactantPhenol, 2-chloro-4-fluoro-5-nitro-HCID 158655—
SolventWaterHCID 962—
Product4-Chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)nitrobenzeneHCID 1461784977.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 2-chloro-4-fluoro-5-nitrophenol (100 g), anhydrous potassium carbonate (86.6 g) and dimethylformamide (500 g) was heated at 50° C., and amyl 2-chloroacetate (90.2 g) was dropwise added thereto in 30 minutes, followed by allowing to stand at 60° C. for 4 hours. The reaction mixture was cooled to room temperature, and water (1500 g) was added thereto, followed by extraction with ethyl acetate (1500 g). The organic layer was separated, washed with water and concentrated under reduced pressure. The residue was distilled under reduced pressure to give 4-chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)nitrobenzene (Compound (III)) (129 g) as a pale yellow oil. Yield, 77%. b.p., 160 °-165° C./0.7 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04987247
Source datasetuspto-grants-1991_01
ORD IDord-7d833a2fbac6442e9b55822269a7a13a
Source noteuspto-grants-1991_01