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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Acetic acid, chloro-, pentyl ester | HCID 138488 | — |
| Reactant | Phenol, 2-chloro-4-fluoro-5-nitro- | HCID 158655 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chloro-2-fluoro-5-(pentyloxycarbonylmethyloxy)nitrobenzene | HCID 14617849 | 77.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04987247 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-7d833a2fbac6442e9b55822269a7a13a |
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| Source note | uspto-grants-1991_01 |
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