HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17789Generated: October 26, 2026
(E)-1,3-Dichloropropene → N-(3-Chloro-allyl)-2,2,2-trifluoro-acetamide
https://huagongshe.com/reaction/17789
Participants
| Role | Name | HCID | Charge |
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| Reactant | (E)-1,3-Dichloropropene | HCID 24726 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Trifluoroacetamide | HCID 67717 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(3-Chloro-allyl)-2,2,2-trifluoro-acetamide | HCID 86761131 | — |
Reaction Steps
Trifluoroacetamide (10.44 g, 92.4 mmol) is dissolved in THF (30 mL). Sodium hydride (60% weight dispersion in mineral oil, 3.1 g, 77 mmol) is then added in small portions at room temperature while regulating the temperature of the reaction with a water bath. The mixture is stirred at room temperature for 5 min., after which E-1,3-dichloropropene (4.5 mL, 49.4 mmol) is added. After 2 min., the mixture thickened, and the reaction was heated to reflux for 45 min. The mixture is then cooled to room temperature, and saturated aqueous ammonium chloride (20 mL) and water (40 mL) are added. The mixture is transferred to a separatory funnel and extracted with ether (2×400 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure to obtained a colorless oil that was used for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741294B1 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-09f05db54e8449f1b33909fca330bb9d |
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| Source note | uspto-grants-2010_06 |
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