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HRID 593728作成日:2026年10月26日

2-Bromothiazole → (3-Bromo-2-fluorophenyl)(thiazol-2-yl)methanol

https://huagongshe.com/reaction/593728

反応式

関与物質

役割名称HCID仕込み量
反応物2-BromothiazoleHCID 76430—
反応物3-Bromo-2-fluorobenzaldehydeHCID 22019361—
反応物HCID 178418918HCID 178418918—
溶媒TetrahydrofuranHCID 8028—
生成物(3-Bromo-2-fluorophenyl)(thiazol-2-yl)methanolHCID 86730392—

反応手順

To a solution of 2-bromothiazole (0.088 mL, 0.985 mmol) in THF (2.99 mL) cooled to 0° C. was added isopropylmagnesium chloride (0.493 mL, 0.985 mmol). After 50 min, 3-bromo-2-fluorobenzaldehyde (0.200 g, 0.985 mmol) was added. The reaction mixture was allowed to warm to room temperature overnight. After 12 hr, the reaction was quenched with saturated aqueous NH4Cl. The reaction mixture was diluted with CH2Cl2. The layers were separated. The aqueous phase was extracted with CH2Cl2 (2×). The organic phases were combined, dried over Na2SO4, filtered, and concentrated to afford the title compound as a brown liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242967B2
出典データセットuspto-grants-2016_01
ORD IDord-2b6f271362fe4e7ba61a23ffd2bf98ee
出典メモuspto-grants-2016_01