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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 265738생성일: 2026년 10월 27일

Acetic Acid → (1R,2S)-(+)-cis-1-Amino-2-indanol

https://huagongshe.com/reaction/265738

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sulfuric AcidHCID 1118—
반응물AcetonitrileHCID 6342—
반응물(1R,2R)-2-bromo-2,3-dihydro-1H-inden-1-olHCID 820607—
용매WaterHCID 962—
생성물(1R,2S)-(+)-cis-1-Amino-2-indanolHCID 2725045—

반응 조건

온도60 °C

반응 단계

Into a 200 ml four-neck flask, 50 ml of acetic acid, 21.3 g (0.1 mol) of trans-(±)-2-bromoindan-1-ol (I), and 4.52 g (0.11 mol) of acetonitrile were introduced. While the mixture was stirred, 12.1 g (0.12 mol) of 97% sulfuric acid was dropwise added thereto at 23°-25° C. in a period of 35 minutes. The crystal totally disappeared. The reaction liquid was further stirred at room temperature for 20 hours. When dispersed into 200 ml of water, the reaction liquid became a white slurry. As this slurry was heated at 60° C. for 6 hours while being stirred, the crystal was totally dissolved. The reaction liquid was cooled to room temperature, washed twice with 100 ml of methylene chloride, and then subjected to liquid separation. When an aqueous solution of 25% sodium hydroxide was added to the water phase to attain a pH of 11, a white crystal was deposited. This crystal was filtered off under reduced pressure, washed with 100 ml of water, and then dried in vacuo to yield 5.33 g of cis-(±)-1-aminoindan-2-ol (I) as a white crystal. Its purity determined by a liquid chromatography was 96.9%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05648534
출처 데이터셋uspto-grants-1997_07
ORD IDord-46ea3e9acc7d4a20a639c2a43e2201df
출처 메모uspto-grants-1997_07