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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349223Generated: November 3, 2026

Chloroform → 5-Bromo-2-{2-[2-(4-trifluoromethyl-phenyl)-vinyl]-oxazol-4-ylmethoxy}-pyrimidine

https://huagongshe.com/reaction/349223

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
ReactantSodium t-butoxideHCID 23676156—
Reactant(2-{2-[4-(Trifluoromethyl)phenyl]ethenyl}-1,3-oxazol-4-yl)methanolHCID 68502458—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-2-{2-[2-(4-trifluoromethyl-phenyl)-vinyl]-oxazol-4-ylmethoxy}-pyrimidineHCID 69489016100%

Reaction Steps

4-Hydroxymethyl-2-[2-(4-trifluoromethyl-phenyl)-vinyl]-oxazole (0.538 g, 2.0 mmol) is dissolved in anhydrous tetrahydrofuran (THF) (10 ml) followed by the addition of NaOtBu (0.231 g, 2.4 mmol). After stirring for 15 min at r.t., 5-bromo-2-chloro-pyrimidine (0.426 g, 2.2 mmol) in THF (5 ml) is added slowly over a period of 10 min and stirred for further 30 min at r.t. Chloroform (25 ml) is added; the mixture is washed with 0.5N hydrochloric acid (HCl) and water, dried over MgSO4 and concentrated in vacuo. After flash column chromatography (100% chloroform) 5-bromo-2-{2-[2-(4-trifluoromethyl-phenyl)-vinyl]-oxazol-4-yl-methoxy}-pyrimidine can be isolated as an off-white solid. Yield 0.60 g (71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179812B2
Source datasetuspto-grants-2007_02
ORD IDord-5c4a0f186777492ca0b5df6c6bfffcd1
Source noteuspto-grants-2007_02