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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557921Generated: October 28, 2026

Tetrahydrofuran → HCID 86602285, compound

https://huagongshe.com/reaction/557921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-tert-butyl 2-methyl (2S)-4-oxopyrrolidine-1,2-dicarboxylateHCID 10988485—
ReactantHCID 178418255HCID 178418255—
SolventDiethyl EtherHCID 3283—
ProductHCID 86602285HCID 86602285—

Reaction Steps

Phenylmagnesium bromide in ether (3.00M, 0.400 mL) was added to a solution of 1-tert-butyl 2-methyl (2S)-4-oxopyrrolidine-1,2-dicarboxylate (243.0 mg, 0.0009989 mol) in tetrahydrofuran (5.00 mL, 0.0616 mol) at −40° C. The reaction mixture was stirred at between −40° C. and −10° C. for 2 h and then was quenched with ammonium chloride solution (5 mL). The organic phase was separated and the aqueous phase was extracted with ethyl acetate (2×5 mL). The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was used directly in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058288B2
Source datasetuspto-grants-2011_11
ORD IDord-522658ca5c544cf1b501b97494678393
Source noteuspto-grants-2011_11