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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677083Generated: October 31, 2026

Tetrahydrofuran → HCID 67372280, compound

https://huagongshe.com/reaction/1677083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 67372399HCID 67372399—
ReactantHCID 178418573HCID 178418573—
ProductHCID 67372280HCID 67372280—

Reaction Steps

Under a nitrogen atmosphere and under ice-cooling, methyl magnesium bromide (20.7 mL, 0.97 M tetrahydrofuran solution) was added dropwise into a tetrahydrofuran (60 mL) solution of (2R,5S)-5-(3,4-difluorophenyl)pyrrolidine-1,2-dicarboxylic acid 1-t-butyl ester 2-ethyl ester (2.5 g). After stirring for 2 hours at the same temperature, ammonium chloride aqueous solution and ethyl acetate were added, and the organic layer was partitioned. The organic layer was washed with brine and dried with magnesium sulfate, and the solvent was removed under a vacuum. Ethyl acetate (7 mL) and 4 N hydrochloric acid/ethyl acetate (20 mL) were added to the residue, and stirring was continued for 1 hour at room temperature. The solvent was removed under a vacuum, and ethyl acetate and sodium bicarbonate aqueous solution were added, and the organic layer was partitioned. The organic layer was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was removed under a vacuum, and the title compound (1.66 g) was obtained. The physical property values are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008293B2
Source datasetuspto-grants-2011_08
ORD IDord-28ebeb9a1572473a8350aa05314ad2f0
Source noteuspto-grants-2011_08