돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 569647생성일: 2026년 10월 25일

p-Toluenesulfonic acid → Pyrrolidine, 1-(6-chloro-3,4-dihydro-2-naphthalenyl)-

https://huagongshe.com/reaction/569647

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물PyrrolidineHCID 31268—
반응물6-Chloro-2-tetraloneHCID 4456139—
용매TolueneHCID 1140—
생성물Pyrrolidine, 1-(6-chloro-3,4-dihydro-2-naphthalenyl)-HCID 10444008—

반응 단계

1155 g (6.4 mol) of 6-chloro-3,4-dihydro-2(1H)-naphthalenone were dissolved in 5 l of toluene, 500 g (7.0 mol) of pyrrolidine and subsequently a solution of 26 g (0.14 mol) of p-toluenesulphonic acid in toluene were added dropwise thereto and the mixture was boiled under reflux. When about 120 ml of water had separated, 4 l of toluene were distilled off and the mixture was left to cool slowly. A solid crystallized out. Filtration and washing with acetone gave 1-(6-chloro-3,4-dihydro-2-naphthyl)pyrrolidine of melting point 117°-118°. Concentration of the mother liquor, suspension of the residue in ether, filtration and washing with acetone gave a further portion of the above product of melting point 117°-118°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04732979
출처 데이터셋uspto-grants-1988_03
ORD IDord-8b2cd8d887db431cba9bbb09b872f1ba
출처 메모uspto-grants-1988_03