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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393010생성일: 2026년 10월 24일

Acetic Anhydride → HCID 22661464, 화합물

https://huagongshe.com/ko/reaction/393010

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물Pentyl nitriteHCID 10026—
반응물18-Crown-6HCID 28557—
반응물Potassium AcetateHCID 517044—
반응물(3-Amino-2-methylphenyl)methanolHCID 577175—
용매ChloroformHCID 6212—
용매DichloromethaneHCID 6344—
생성물HCID 22661464HCID 22661464—

반응 단계

Acetic anhydride (1.68 mL, 17.8 mmol) was added to a suspension of 3-amino-2-methylbenzyl alcohol (0.82 g, 5.98 mmol) in chloroform (25 mL). Potassium acetate was added and the resulting mixture was stirred at room temperature for 3 h, under reflux for 2 h, and then at room temperature overnight. Amyl nitrite (1.82 mL, 13.7 mmol) and 18-crown-6 (79 mg, 0.3 mmol) were added and the pale yellow cloudy mixture was heated at reflux overnight, then allowed to cool to room temperature and stir for 5 h. The reaction mixture was poured into acetic anhydride (5 mL) and stirred at room temperature overnight. Dichloromethane (20 mL) was added and the solution was washed with sodium hydrogen carbonate solution, water, and brine (10 mL each), dried (Na2SO4), filtered, concentrated, and chromatographed (10-40% ethyl acetate/petroleum ether) to give 1-acetyl-1H-indazole-4-methanol, acetate ester (1.19 g, 86%) as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06803384B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-b39cff47faa040efb41e1c8e294a47ef
출처 메모uspto-grants-2004_10