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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624224Generated: November 3, 2026

Carbon Dioxide → 6-Bromo-2-methylthieno[3,4-d][1,3]oxazole

https://huagongshe.com/reaction/1624224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantSodium ChlorideHCID 5234—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Methylthieno[3,4-d][1,3]oxazoleHCID 68242274—
SolventTetrahydrofuranHCID 8028—
Product6-Bromo-2-methylthieno[3,4-d][1,3]oxazoleHCID 68242295—

Reaction Steps

1 mmol of 2-methylthieno[3,4-d][1,3]oxazole was dissolved in 10 ml of tetrahydrofuran and the temperature was kept at −78° C. in a methanol bath cooled by dry ice. A solution in which 1.05 mmol of N-bromosuccinimide was dissolved in 5 ml of tetrahydrofuran was gradually added dropwise to carry out the reaction for 2 hours. Then an excess amount of saturated sodium chloride aqueous solution was added to stop the reaction. The reacted liquid was washed with water. Then the organic layer was recovered and dried under sodium sulfate. The solvent was evaporated out. The product was purified using column separation with the solvent of ethylacetate and hexane, obtaining 6-bromo-2-methylthieno[3,4-d][1,3]oxazole represented by formula (21).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08779086B2
Source datasetuspto-grants-2014_07
ORD IDord-7f3fdd325a44432fb70c3956b9f1b2f2
Source noteuspto-grants-2014_07