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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993820Generated: October 26, 2026

Hydrochloric Acid → 2-Cyano-2-[4-(2,5-dichloro-phenoxy)-3-fluoro-phenylthiocarbamoyl]-acetamide

https://huagongshe.com/reaction/1993820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCyanoacetamideHCID 7898—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant4-(2,5-Dichloro-phenoxy)-3-fluoro-phenylisothiocyanateHCID 59797663—
SolventTetrahydrofuranHCID 8028—
Product2-Cyano-2-[4-(2,5-dichloro-phenoxy)-3-fluoro-phenylthiocarbamoyl]-acetamideHCID 5979770882.5%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of potassium tert-butoxide (0.6 g, 5.36 mmol) in 10 ml of anhydrous THF was added 2-cyanoacetamide (0.45 g, 5.36 mmol) under argon. The mixture was cooled to 5° C. and added dropwise to a solution of 4-(2,5-dichloro-phenoxy)-3-fluoro-phenylisothiocyanate (1.53 g, 4.87 mmol) in 5 ml of dry THF with stirring under argon. After 15 min of stirring at 5° C., this reaction mixture was warmed to room temperature and stirred for another 2 h. The reaction mixture was poured into 200 ml of ice water with stirring and acidified with 10% HCl. The solid was filtered and washed with water. After drying in vacuo, the crude product (1.6 g, 82.5%) was obtained in sufficient purity for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652047B2
Source datasetuspto-grants-2010_01
ORD IDord-5dffbfc5eac7434a90c04c7d1a7ccc66
Source noteuspto-grants-2010_01