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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 423106생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/423106

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Bromocresol GreenHCID 6451—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물(Z)-1-(4-chlorophenyl)-2-(thiazol-2-yl)ethenamineHCID 57750306—
용매MethanolHCID 887—
생성물1-(4-Chlorophenyl)-2-(thiazol-2-yl)ethanamineHCID 5775029290%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101623B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-515c8603d63a4e06b4bcd8fad7ec7bd3
출처 메모uspto-grants-2012_01