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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599991Generated: November 3, 2026

Tetrahydrofuran → HCID 53986092, compound

https://huagongshe.com/reaction/1599991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantCyanamide, 2-propenyl-HCID 12295222—
ReactantHCID 53725594HCID 53725594—
ProductHCID 53986092HCID 53986092—

Reaction Conditions

Temperature55 °C

Reaction Steps

0.36 g (4.4 mmol) of allylcyanamide were added to a suspension of 2 g (4.4 mmol) of 2-chloro-3-(2,4-dichloro-5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)phenyl)Propenoyl chloride and 0.8 g (5.8 mmol) of potassium carbonate(ground) in 50 ml of tetrahydrofuran. The reaction mixture was stirred at 50 to 60° C. for 5 hours and then concentrated. The residue was taken up in ethyl acetate, after which the organic phase was washed with water, dried over magnesium sulfate and concentrated. The crude product was purified by means of column chromatography on silica gel (eluent: ethyl acetate) followed by crystallization from diisopropyl ether. Yield: 0.2 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05744426
Source datasetuspto-grants-1998_04
ORD IDord-91bc213efd4b4ce8b0f2c6135cf38971
Source noteuspto-grants-1998_04