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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061262Generated: November 4, 2026

Borane → HCID 54321631, compound

https://huagongshe.com/reaction/1061262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoraneHCID 6331—
Reactant(R)-2-Methyl-CBS-oxazaborolidineHCID 9838490—
ReactantHCID 10978660HCID 10978660—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54321631HCID 5432163166.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Borane (in THF, 1M, 10.35 mL, 10.5 mmol) was added dropwise into a mixture of (R)-2-methyl-CBS-oxazaborolidine monohydrate (0.38 g, 1.31) mmol and tetrahydrofuran (15 mL) under a nitrogen atmosphare at ambient temperature. The mixture was stirred for 10 minutes and then 2-bromo-1-[2-(trifluoromethyl)-1,3-thiazole-4-yl]ethanone (which was obtained in Example 102) (3.6 g, 13.13 mmol) in tetrahydrofuran (20 mL) was added dropwise over 10 minutes. The new mixture was stirred at room temperature for 4 hours. The reaction mixture was cooled to 0° C. and quenched with a hydrogen chloride/ethyl ether solution (1M, 1.0 mL). After stirring at 0° C. for 30 minutes, H2O (20 mL) was added dropwise and the mixture was extracted with ethyl ether. The organic layer was washed with aqueous ammonium chloride and dried over MgSO4. Evaporation and purification by flash chromatography (hexanes/dichloromethane/ethanol 1/1/0.01) gave a clear oil (2,4 g, 66% yield); MS (ES) m/z: 334/336 (M+acetic acid−H)−; 1H NMR (400 MHz, CDCl3) δ 2.94 (m, 1H), 3.74 (m, 1H), 3.94 (m, 1H), 5.16 (m, 1H), 7.62 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525202B2
Source datasetuspto-grants-2003_02
ORD IDord-3d69fb8d3c50419aa8227bb884c357cf
Source noteuspto-grants-2003_02