Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557894Generated: November 1, 2026

Thiazole → HCID 59298225, compound

https://huagongshe.com/reaction/557894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazoleHCID 9256—
ReactantTert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 59298225HCID 5929822570.4%

Reaction Steps

1.600 M of n-Butyllithium in hexane (1.0×10−1 mL) was added to 1,3-thiazole (0.958 mL, 0.0135 mol) in THF (20 mL) at −78° C. After 30 minutes, tert-butyl 3-oxopyrrolidine-1-carboxylate (2.50 g, 0.0135 mol) in THF (10 mL) was added, and the mixture was slowly warmed to room temperature overnight. The reaction was quenched with water, and the reaction mixture was extracted with ethyl acetate, dried with MgSO4, filtered and concentrated. The residue was purified by flash column (50% EtOAc/hexanes to pure EtOAc) to give the desired product (2.57 g, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058288B2
Source datasetuspto-grants-2011_11
ORD IDord-7dbf28b5dad3481eac69594b652fb1bd
Source noteuspto-grants-2011_11