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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426497Generated: November 4, 2026

Tetrahydrofuran → HCID 13620271, compound

https://huagongshe.com/reaction/1426497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAcetylacetoneHCID 31261—
ReactantDimethylformamide dimethyl acetalHCID 78373—
ReactantBenzylhydrazine dihydrochlorideHCID 146540—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 13620271HCID 1362027163.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of pentane-2,4-dione (10.01 g) and 1,1-dimethoxy-N,N-dimethylmethanamine (12.51 g) was stirred at 80° C. for 1 hr. Tetrahydrofuran (20 mL) was added to the reaction mixture, benzylhydrazine dihydrochloride (21.46 g) was added by small portions under ice-cooling, and the mixture was stirred at 60° C. for 30 min. The reaction mixture was allowed to cool to room temperature, ethyl acetate (100 mL) and water (100 mL) were added, and the separated aqueous layer was extracted with ethyl acetate (50 mL×2). The combined organic layers were washed with brine (20 mL) and dried over anhydrous magnesium sulfate. Insoluble material was removed by filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title to compound (13.53 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933069B2
Source datasetuspto-grants-2015_01
ORD IDord-08fd69171e894c6db65a2ef9a7a3b267
Source noteuspto-grants-2015_01