HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850665Generated: October 30, 2026
Water → Allyl 3-amino-4,4,4-trichloro-2-cyanobut-2-enoate
https://huagongshe.com/reaction/1850665
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Trichloroacetonitrile | HCID 11011 | — |
| Reactant | Allyl cyanoacetate | HCID 25919 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Allyl 3-amino-4,4,4-trichloro-2-cyanobut-2-enoate | HCID 86720886 | — |
Reaction Steps
To a solution of KOAc (589.4 g, 6.006 mol) in isopropanol (3 L) was added allyl cyanoacetate (429.4 g, 403.2 mL, 3.432 mol) and the reaction mixture was cooled to 5° C. Trichloroacetonitrile (495.5 g, 3.432 mol) was added in 50 mL portions, maintaining temperature below 15° C. The reaction mixture was then allowed to warm to 20° C. and stirred for 3 h. Water (˜4 L) was added to dissolve the inorganic materials and precipitate out the desired product. The mixture was stirred for 20 minutes and the solid was isolated by filtration under vacuum. This solid was filtered, washed with water (2×0.5 L) and dried in a vacuum oven overnight at 40° C. to afford allyl 3-amino-4,4,4-trichloro-2-cyanobut-2-enoate 2 as an off-white powder (787 g, 85%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957078B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-218afb73c0b34b5b9afde5157d2004ce |
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| Source note | uspto-grants-2015_02 |
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