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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41673Generated: October 25, 2026

Triglyme → 5-{1-[2-(4-Bromo-2-methyl-phenyl)-thiazol-5-yl]-ethoxy}-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one

https://huagongshe.com/reaction/41673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriglymeHCID 8189—
ReactantSodium hydrideHCID 24758—
Reactant1-[2-(4-Bromo-2-methyl-phenyl)-thiazol-5-yl]-ethanolHCID 59584676—
Reactant5-Chloro-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-oneHCID 68567844—
SolventTetrahydrofuranHCID 8028—
Product5-{1-[2-(4-Bromo-2-methyl-phenyl)-thiazol-5-yl]-ethoxy}-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-oneHCID 6877358573.2%

Reaction Steps

To a solution of [2-(4-bromo-2-methyl-phenyl)-thiazol-5-yl]-ethanol (450 mg, 1.5 mmol) and 5-chloro-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one (277 mg, 1.5 mmol) in tetrahydrofuran (10 ml) is added in one portion the sodium hydride (60% dispersion in mineral oil, 60 mg, 1.5 mmol). The reaction mixture is stirred at room temperature for 24 hours. The crude reaction mixture is vacced down under reduced pressure and 10 ml of triglyme are added. The reaction mixture is therefore heated to reflux for 30 minutes. The crude reaction mixture is vacced down and purified by flash chromatography on silica gel to give a yellow solid. The solid is washed with iso-hexane to give 5-{1-[2-(4-bromo-2-methyl-phenyl)-thiazol-5-yl]-ethoxy}-10-oxa-tricyclo[5.2.1.0*2,6*]dec-4-en-3-one (490 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530667B2
Source datasetuspto-grants-2013_09
ORD IDord-d1656d9515194173a1d6413fd2f90966
Source noteuspto-grants-2013_09