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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 976288생성일: 2026년 10월 24일

1,2-Dimethoxyethane → 1-Azabicyclo(2.2.2)octane-3-carbonitrile

https://huagongshe.com/ko/reaction/976288

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물3-QuinuclidinoneHCID 19507—
반응물1-Isocyanatomethanesulfonyl-4-methylbenzeneHCID 11789078—
반응물Potassium tert-butoxideHCID 23665647—
용매EthanolHCID 702—
생성물1-Azabicyclo(2.2.2)octane-3-carbonitrileHCID 14286574.5%

반응 단계

A solution of potassium tert-butoxide (18.27 ml) in 1:1 (v/v) mixture of dimethoxyethane and ethanol (100 ml) was added slowly to a stirred mixture of 3-quinuclidinone (8.14 g), tosylmethylisocyanate (16.53 g) in dry ethanol (6.5 ml), and dry dimethoxyethane (228 ml) under an atmosphere of argon whilst maintaining the temperature below 10° C. The reaction mixture was allowed to warm to ambient temperature and stirred at this temperature for 30 minutes. The reaction mixture was then stirred at 40° C. for 3 hours. The reaction mixture was cooled, filtered and the filtrate evaporated. The residue was purified by flash column chromatography on alumina (Brockmann Grade I) using a 2:98 (v/v) mixture of methanol/ethyl acetate as eluant to give 3-cyanoquinuclidine (6.6 g), microanalysis, found: C, 67.6; H, 8.5; N, 18.7%; C8H12N2 requires: C, 70.6; H, 8.8; N, 20.6%; NMR (CDCl3): 1.4-1.7 (3H, m), 1.85-2.0 (1H, m) 2.0-2.1 (1H, m) and 2.6-3.4 (7H, m); m/z 137 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05612352
출처 데이터셋uspto-grants-1997_03
ORD IDord-674cbd93d49343d395987c36d51fabd6
출처 메모uspto-grants-1997_03