HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429477Generated: October 29, 2026
Oxalyl chloride → (S)-2-(4-fluorophenyl)pent-4-enoyl chloride
https://huagongshe.com/reaction/429477
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | (2S)-2-(4-fluorophenyl)pent-4-enoic acid | HCID 15536021 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-2-(4-fluorophenyl)pent-4-enoyl chloride | HCID 15536025 | — |
Reaction Steps
Combine (S)-2-(4-fluorophenyl)pent-4-enoic acid (3.61 g, 18.6 mmol), dichloromethane (20 mL), and dimethylformamide (2 drops). Add oxalyl chloride (1.94 mL, 22.3 mmol). After 2 hours, evaporate in vacuo to give (S)-2-(4-fluorophenyl)pent-4-enoyl chloride. Combine with toluene (10 mL) and slowly add, with vigorous stirring, to a cooled (ice bath) aqueous solution of methylamine (4 mL, 40%). After 1 hour, partition the reaction mixture between water and dichloromethane. Separate the layers, extract the organic layer with a saturated aqueous sodium bicarbonate solution. Dry the organic over MgSO4, filter, and evaporate in vacuo to give a residue. Triturate the residue with hexane to give a solid. Collect the solid by filtration and dry to give (S)-2-(4-fluorophenyl)pent-4-enoic acid, N-methyl amide: mp; 104-105° C. Rf=0.42 (silica gel, 50% ethyl acetate/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06316445B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-f2e264cde3934506b3119c20974bf584 |
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| Source note | uspto-grants-2001_11 |
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