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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341973Generated: October 26, 2026

1,3-Dichloroacetone → HCID 178511217, compound

https://huagongshe.com/reaction/341973

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DichloroacetoneHCID 10793—
Reactant3-ChloropropionitrileHCID 10963—
ReactantSodium HydroxideHCID 14798—
ReactantThioureaHCID 2723790—
ReactantAmidinothioureaHCID 2724563—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 178511217HCID 17851121761.1%

Reaction Conditions

Temperature10 °C

Reaction Steps

Into a 500 mL round bottom flask equipped with an overhead stirrer and under an inert atmosphere was added 25 g of 1,3-dichloroacetone (0.197 mol) and 75 g of acetone. The reaction mixture was cooled to 10° C. and 23.2 g 2-imino-4-thiobiuret (0.197 mol) was added. The reaction mixture was stirred for one hour at 10 C. The reaction mixture was then heated to 40° C. and 15 g of thiourea (0.197 mol) was added, followed by the addition of 100 g of water. The mixture was heated to and held at 52° C. for one hour. Acetone was then removed by vacuum distillation. To the reaction mixture was added 100 g of water, 17 g of 3-chloropropionitrile (0.190 mol) and 40 g of isopropyl alcohol. The reaction mixture was cooled below 10° C. and 25 g of an aqueous solution of sodium hydroxide (80 g water) was added dropwise maintaining the reaction temperature below 10° C. The reaction mixture was for 2 hours, filtered and washed to produce 28 g of N-[4-(cyanoethylthiomethyl)-2-thiazolyl]guanidine product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856500
Source datasetuspto-grants-1999_01
ORD IDord-f3466171283b4e8baa7b035687e671be
Source noteuspto-grants-1999_01