Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408493Generated: October 25, 2026

Tetrahydrofuran → HCID 58609916, compound

https://huagongshe.com/reaction/408493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-(2-Methoxyphenyl)acetaldehydeHCID 269548—
Reactanttert-butyl 2-amino-2H-1,3-thiazole-3-carboxylateHCID 66545324—
ReactantButyllithiumHCID 178418339—
ProductHCID 58609916HCID 5860991628%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of n-butyl lithium (2.5 M, 250 mL, 0.62 mol) was added to a solution of N-Boc-2-aminothiazole (56 g, 0.28 mol) in anhydrous tetrahydrofuran (500 mL) was added at −78° C. After the addition was completed, the mixture was allowed to stir at −78° C. for one hour. A solution of (2-methoxy-phenyl)-acetaldehyde (36 g, 0.24 mol) in tetrahydrofuran (100 mL) was slowly added to the reaction mixture while maintaining a temperature of −78° C. The mixture was allowed to warm to room temperature and stirred for 15 hours. The reaction was quenched with a saturated aqueous solution of ammonium chloride (1000 mL) and extracted three times with ethyl acetate (400 mL). The combined organic layers were washed with a saturated aqueous solution of sodium chloride, dried over sodium sulfate, and evaporated to dryness. The crude product was purified by column chromatography to give the pure product (28 g, 0.080 mol, 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759335B2
Source datasetuspto-grants-2014_06
ORD IDord-6c33cdf1efe14b06bbd2feaa337fc178
Source noteuspto-grants-2014_06