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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 504424Generated: November 3, 2026

Tetrahydrofuran → HCID 66662607, compound

https://huagongshe.com/reaction/504424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Butene, 1-bromo-3-methyl-HCID 70092—
ReactantTert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
CatalystZincHCID 23994—
ProductHCID 66662607HCID 66662607—

Reaction Steps

To a suspension of tert-butyl 3-oxopyrrolidine-1-carboxylate (2.40 g, 0.0130 mol), 4-bromo-2-methyl-2-butene (3.00 mL, 0.0260 mol) in 15.0 mL sat'd. ammonium chloride and tetrahydrofuran (3.00 mL, 0.0370 mol) was added zinc (1.70 g, 0.0260 mol) at rt. Soon after stirring was started, gas and heat were released. After 30 to 45 min., the resulting light grey mixture was filtered through celite. The filtration was extracted with EtOAc. The organic layers were combined, washed with brine, dried (NaSO4) and concentrated in-vacuo. The residue was purified on silica gel, eluting with 0 to 40% EtOAc in hexane, to give the desired product. LCMS (M+Na) 278.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776874B2
Source datasetuspto-grants-2010_08
ORD IDord-2abcbc3f683f46e19421af28dfb5026c
Source noteuspto-grants-2010_08