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HRID 1044753作成日:2026年10月26日

Nitrogen → 2-Bromo-5-(2-methyl-[1,3]dioxolan-2-yl)-thiazole

https://huagongshe.com/reaction/1044753

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物Trimethyl orthoformateHCID 9005—
反応物Sodium BicarbonateHCID 516892—
反応物1-(2-Bromo-1,3-thiazol-5-yl)ethan-1-oneHCID 57562813—
溶媒Ethylene GlycolHCID 174—
生成物2-Bromo-5-(2-methyl-[1,3]dioxolan-2-yl)-thiazoleHCID 66820078—

反応条件

温度95 °C

反応手順

In a flame dried round-bottomed flask equipped with a magnetic stir bar and a condenser under inert atmosphere (N2), a solution of 1-(2-bromo-thiazol-5-yl)-ethanone (16.22 g, 78.71 mmol) in ethylene glycol (85 mL) was treated with trimethylorthoformate (18 mL, 164.19 mmol) followed by LiBF4 (1.51 g, 15.74 mmol). The reaction mixture was heated at 95° C. for 2 days. Sat. aq. NaHCO3 was added and the mixture was extracted with Et2O (3×). The org. extracts were washed with brine, dried over MgSO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (20:1 to 3:1 hept-EA) gave the title compound as a yellow solid. TLC:rf (1:1 hept-EA)=0.63. LC-MS-conditions 02: tR=0.89 min; [M+H]+=250.24.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08563714B2
出典データセットuspto-grants-2013_10
ORD IDord-310be4375919419b9130be1b8e51e298
出典メモuspto-grants-2013_10