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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869109Generated: October 31, 2026

Water → Allyl 3-amino-4,4,4-trichloro-2-cyanobut-2-enoate

https://huagongshe.com/reaction/869109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrichloroacetonitrileHCID 11011—
ReactantAllyl cyanoacetateHCID 25919—
ReactantPotassium AcetateHCID 517044—
SolventIsopropanolHCID 3776—
ProductAllyl 3-amino-4,4,4-trichloro-2-cyanobut-2-enoateHCID 86720886—

Reaction Conditions

Temperature5 °C

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%). 1H NMR (500 MHz, CDCl3) δ 10.17 (br s, 1H), 6.97 (m, 1H), 5.99 (m, 1H), 5.44 (m, 1H), 5.31 (m, 1H), 4.76 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969360B2
Source datasetuspto-grants-2015_03
ORD IDord-80c90be3432c43d499fab2970c59ebf5
Source noteuspto-grants-2015_03