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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488172Generated: November 2, 2026

3-Furancarboxamide,tetrahydro-N-methoxy-N-methyl-(9CI) → HCID 21702750, compound

https://huagongshe.com/reaction/1488172

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Furancarboxamide,tetrahydro-N-methoxy-N-methyl-(9CI)HCID 45084522—
ReactantHCID 178418443HCID 178418443—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21702750HCID 2170275083.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a 250-mL 3-neck round-bottom flask, was placed a solution of N-methoxy-N-methyltetrahydrofuran-3-carboxamide (compound 263.1, 6.71 g, 42.2 mmol) in tetrahydrofuran (100 mL). The system was purged with nitrogen, then cooled to 0° C. Ethylmagnesium bromide (3M in diethyl ether, 17 mL, 51 mmol) was added drop-wise at 0° C. over 30 min. The resulting solution was stirred overnight at 40° C., then cooled and carefully quenched with aqueous HCl (1M, 10 mL). The resulting mixture was concentrated under reduced pressure and the residue was diluted with water (10 mL). The mixture was extracted with ethyl acetate (3×30 mL) and the combined organic extracts were washed with brine (2×10 mL), dried (Na2SO4), filtered and concentrated under reduced pressure. Obtained the title compound as a light yellow oil (4.5 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428502B2
Source datasetuspto-grants-2016_08
ORD IDord-2822da7dd25c4ff09cc8fcfb5a8309b2
Source noteuspto-grants-2016_08