戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 10399作成日:2026年10月24日

Sodium borohydride → 5-Bromo-2-benzothiazoleethanol

https://huagongshe.com/ja/reaction/10399

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物Ethyl 2-(5-bromobenzo[D]thiazol-2-YL)acetateHCID 21041508—
溶媒EthanolHCID 702—
溶媒TetrahydrofuranHCID 8028—
生成物5-Bromo-2-benzothiazoleethanolHCID 21980060—

反応手順

(5-Bromo-benzothiazol-2-yl)-acetic acid ethyl ester (1.25 g, 4.2 mmol) was dissolved in THF (20 mL) and EtOH (5 mL) under N2. Then 0.24 g of NaBH4 was dissolved in EtOH (3 mL) and added to the above solution. The reaction mixture was stirred at room temperature for 2 hours. After the completion the mixture was quenched with water and extracted with CH2Cl2. The aqueous layer was extracted again with more CH2Cl2. The combined methylene chloride layer was dried over anhydrous MgSO4 and filtered. Removal of solvent gave crude product with a yield of 1.11 g. The crude product was used directly in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094790B2
出典データセットuspto-grants-2006_08
ORD IDord-98cc223bf38a4ce9a090aa143a53649e
出典メモuspto-grants-2006_08