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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1614249생성일: 2026년 10월 26일

Hydrochloric Acid → HCID 19773292, 화합물

https://huagongshe.com/reaction/1614249

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-Thiopheneethylamine, hydrochlorideHCID 458572—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물5-Acetylamino-2-tetraloneHCID 14836456—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물HCID 19773292HCID 19773292—

반응 단계

2.03 g of (0.01 mol) of 5-acetylamino-2-tetralone, 3.2 g (0.02 mol) of 2-(2-thienyl)-ethyl-aminehydrochloride and 0.75 g (0.012 mol) of sodium cyanoborohydride are dissolved in 30 ml of methanol and stirred for 24 hours at ambient temperature. The mixture is then acidified by the dropwise addition of conc. hydrochloric acid with stirring and cooling with ice. After 10 minutes, 100 ml of water is added whilst stirring continues and then a total of 4.0 g of anhydrous soda is added in batches. Then extraction is carried out with 50 ml of methylene chloride and twice with 25 ml of methylene chloride. The combined extracts are washed with 20 ml of water, dried with sodium sulphate and after separation of the drying agent, concentrated by evaporation in a rotary evaporator, finally at 90° C. and under a complete water-jet vacuum. The residue is dissolved with 5 ml of methanol and 4.0 ml of 2.5 N ethanolic hydrochloric acid and the solution is mixed with diethylether until turbidity is just beginning. After standing for a period of about 12 hours at 5° C. the title compound is suction filtered, washed with ethanol/ether and dried at 80° C. until the weight remains constant. Yield: 3.1 g (88.3% of theory), melting point 276° C. (unchanged after recrystallisation from methanol/ether).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05196454
출처 데이터셋uspto-grants-1993_03
ORD IDord-d5a8b3f7b2c645b698bc401246eb4743
출처 메모uspto-grants-1993_03