HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599625Generated: October 30, 2026
Oxalyl chloride → 4-Chloro-2-(3,4,5-trifluorophenyl)butyryl chloride
https://huagongshe.com/reaction/599625
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4-Chloro-2-(3,4,5-trifluorophenyl)butyric acid | HCID 66839530 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Chloro-2-(3,4,5-trifluorophenyl)butyryl chloride | HCID 86615146 | — |
Reaction Steps
oxalyl chloride (0.63 mL) and DMF (1 drop) were added to a solution of 4-chloro-2-(3,4,5-trifluorophenyl)butyric acid (1.17 g) in methylene chloride (30 mL) at 0° C., and the reaction solution was stirred at room temperature for one hour. The reaction solution was concentrated under reduced pressure to obtain 4-chloro-2-(3,4,5-trifluorophenyl)butyryl chloride. A solution of 4-chloro-2-(3,4,5-trifluorophenyl)butyryl chloride in THF (5 mL) was added to a solution of tert-butyl carbazate (600 mg) and triethylamine (3.1 mL) in THF (20 mL) at 0° C., and the reaction solution was stirred at room temperature for one hour. The reaction solution was added to a saturated sodium bicarbonate solution, followed by extraction with ethyl acetate. The resulting extract was dried over magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: heptane-ethyl acetate system) to obtain 1.35 g of the title compound. The property value of the compound is as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897632B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-bc6797e5b58b4df2b22e7e6455449a9b |
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| Source note | uspto-grants-2011_03 |
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