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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909432Generated: November 3, 2026

Sodium hydride → HCID 66742678, compound

https://huagongshe.com/reaction/1909432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(2-Bromo-1,3-thiazol-5-yl)methanolHCID 7213124—
ReactantHCID 57591516HCID 57591516—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66742678HCID 6674267881.9%

Reaction Steps

To a solution of (2-bromothiazol-5-yl)methanol (4.85 g, 25 mmol) and 4-chloro-bicyclo[3.2.1]oct-3-en-2-one (3.92 g, 25 mmol) in anhydrous tetrahydrofuran (100 ml) is added, in small portions, sodium hydride (60% dispersion in oil, 1.00 g, 25 mmol) at 0° C. The reaction mixture is stirred overnight and allowed to warm to room temperature. Silica gel is added to the crude reaction mixture, the solvent is evaporated under reduced pressure and the residue is purified by flash chromatography on silica gel to give 4-(2-bromothiazol-5-ylmethoxy)bicyclo[3.2.1]oct-3-en-2-one (6.43 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598365B2
Source datasetuspto-grants-2013_12
ORD IDord-8bced1a43f2748f580a7ee8929536a20
Source noteuspto-grants-2013_12