戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1040086作成日:2026年10月27日

Methyl iodide → 5-Bromo-2-[2-(methylsulfonyl)propan-2-yl]-1,3-thiazole

https://huagongshe.com/reaction/1040086

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Sodium MethoxideHCID 10942334—
反応物Methyl 3-{[2-(5-bromo-1,3-thiazol-2-yl)propan-2-yl]sulfonyl}propanoateHCID 67258095—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物5-Bromo-2-[2-(methylsulfonyl)propan-2-yl]-1,3-thiazoleHCID 6725857493.3%

反応手順

Methyl 3-{[2-(5-promo-1,3-thiazol-2-yl)propan-2-yl]sulfonyl}propanoate (Example 70, Step 4, 500 mg, 1.403 mmol) was taken up in THF (15 mL) at room temperature, and NaOMe (25% in MeOH, 303 mg, 1.403 mmol) was added. After 30 min at room temperature, the suspension was evaporated to dryness, providing a white solid. The solid was taken back up in DMSO (5 mL), and methyl iodide (398 mg, 2.81 mmol) was added. After stirring for 2 h at room temperature, the reaction was diluted with water and extracted with ethyl acetate (2×). The combined organic layers were washed with brine, dried (MgSO4), filtered and evaporated. Flash chromatography (0-40% ethyl acetate in hexanes) afforded of 5-bromo-2-[2-(methylsulfonyl)propan-2-yl]-1,3-thiazole (372 mg, 93%) as a colorless solid. MS ESI: [M+H]+ m/z 283.9/285.9.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08551984B2
出典データセットuspto-grants-2013_10
ORD IDord-4e1f2f3564b041f38fecf7a8e6b51b5a
出典メモuspto-grants-2013_10