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HRID 423106作成日:2026年10月25日

Hydrochloric Acid → 1-(4-Chlorophenyl)-2-(thiazol-2-yl)ethanamine

https://huagongshe.com/reaction/423106

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Bromocresol GreenHCID 6451—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物(Z)-1-(4-chlorophenyl)-2-(thiazol-2-yl)ethenamineHCID 57750306—
溶媒MethanolHCID 887—
生成物1-(4-Chlorophenyl)-2-(thiazol-2-yl)ethanamineHCID 5775029290%

反応手順

A 2N solution of hydrochloric acid in MeOH at room temperature, was added dropwise to (Z)-1-(4-chlorophenyl)-2-(thiazol-2-yl)ethenamine (Intermediate 94) (1.45 g, 6.13 mmol) and traces of bromocresol green dissolved in MeOH (45 mL) until the solution turned from dark blue to orange. Sodium cyanoborohydride (0.481 g, 7.66 mmol) was added in one portion to the stirred solution and orange color was maintained by adding dropwise the 2N solution of hydrochloric acid in methanol at room temperature. After 1 h stirring, solvent was removed under vacuum. the crude was taken up into water, pH was adjusted around 2 by adding a few drops of the 2N solution of hydrochloric acid in methanol. The aqueous phase was washed with diethyl ether twice then pH was adjusted to 14 by adding a 6N aqueous solution of sodium hydroxide and the basic aqueous phase was extracted with diethyl ether twice. The organic phases were washed with brine dried over magnesium sulphate and concentrated to afford 1-(4-chlorophenyl)-2-(thiazol-2-yl)ethanamine (1.310 g, 90%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101623B2
出典データセットuspto-grants-2012_01
ORD IDord-515c8603d63a4e06b4bcd8fad7ec7bd3
出典メモuspto-grants-2012_01