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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 259358생성일: 2026년 10월 24일

1-(2-Chloroethyl)pyrrolidine → 4-Adamantoyloxy-N-methyl-N-(2-pyrrolidinoethyl)aniline Dihydrochloride Dihydrate

https://huagongshe.com/ko/reaction/259358

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-Chloroethyl)pyrrolidineHCID 81669—
반응물N-Methyl-p-(1-adamantyloxy)anilineHCID 12510299—
반응물4-adamantyloxy-N-methyl-N-(2-pyrrolidinoethyl)aniline dihydrochloride dihydrateHCID 20342199—
반응물ButyllithiumHCID 178418339—
용매BenzeneHCID 241—
용매MethanolHCID 887—
용매TolueneHCID 1140—
용매PentaneHCID 8003—
용매TetrahydrofuranHCID 8028—
생성물4-Adamantoyloxy-N-methyl-N-(2-pyrrolidinoethyl)aniline Dihydrochloride DihydrateHCID 70588067—

반응 단계

To an ice:MeOH cooled solution of 2.0 g. (0.0078 mole) of N-Methyl-p-(1-adamantyloxy)aniline in 20 ml. THF was added 4.75 ml. of 1.64N BuLi in pentane. A solution of a 1:1 mixture of toluene, and 1-chloro-2-pyrrolidino ethane (2.08 g.) in 20 ml. THF was then added and the mixture stirred at room temperature for 1 hour and at reflux for 18 hours. The solution was allowed to cool, diluted with C6H6 and washed with H2O and brine. The residue remaining when the organic fraction was taken to dryness was dissolved in CH2Cl2, treated with 10 ml. HCl saturated Et2O and taken to dryness. The residual solid was recrystallized from CH2Cl2 :CH3CN to yield 1.93 g. (55%) of 4-adamantyloxy-N-methyl-N-(2-pyrrolidinoethyl)aniline dihydrochloride dihydrate, m.p. 189°-190° (efervess).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04036977
출처 데이터셋uspto-grants-1977_07
ORD IDord-77d61c5ff56a4c22b27a5758b6298f8a
출처 메모uspto-grants-1977_07