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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052235Generated: October 30, 2026

Tetrahydrofuran → HCID 28743251, compound

https://huagongshe.com/reaction/1052235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAcetylacetoneHCID 31261—
ReactantDimethylformamide dimethyl acetalHCID 78373—
Reactanttert-Butylhydrazine monohydrochlorideHCID 81889—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 28743251HCID 28743251—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of pentane-2,4-dione (5.01 g) and 1,1-dimethoxy-N,N-dimethylmethanamine (6.26 g) was stirred at 80° C. for 1 hr. Tetrahydrofuran (10 mL) was added to the reaction mixture, tert-butylhydrazine hydrochloride 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 compound (7.47 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388195B2
Source datasetuspto-grants-2016_07
ORD IDord-9260439add904cf39012475ce5abe601
Source noteuspto-grants-2016_07