Pyrrolidine → 1-(6-Bromo-3,4-dihydronaphthalen-2-yl)pyrrolidine

HRID 1379062노트

반응식

HRID 1379062 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8](=O)[CH2:7][CH2:6][CH2:5]2.[NH:13]1[CH2:17][CH2:16][CH2:15][CH2:14]1>C1(C)C=CC=CC=1>[N:13]1([C:7]2[CH2:6][CH2:5][C:4]3[C:9](=[CH:10][CH:11]=[C:2]([Br:1])[CH:3]=3)[CH:8]=2)[CH2:17][CH2:16][CH2:15][CH2:14]1

참가 물질

4

반응물 2

HCID 31268PyrrolidineHCID 101050696-Bromo-1-tetralone

생성물 1

HCID 221654851-(6-Bromo-3,4-dihydronaphthalen-2-yl)pyrrolidine수율 97.4%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

To a 250 ml round bottomed flask was added 5.00 g (22.21 mmol) of the 6-bromotetralone afforded above in Step B; 70 ml of dry toluene and 3.1 g (3.7 ml) of pyrrolidine. The flask was equipped with a Dean-Stark trap, a condenser, a nitrogen inlet tube and a magnetic stirrer and the reaction refluxed for four hours. The solvent was evaporated under vacuum to afford 6.02 g (97.4%) of the subtitle compound as a brown crystalline material which was used without further purification.

후처리

  1. customafforded above in Step B
  2. customThe flask was equipped with a Dean-Stark trap, a condenser, a nitrogen inlet tube and a magnetic stirrer
  3. temperaturethe reaction refluxed for four hours
  4. customThe solvent was evaporated under vacuum

출처 및 근거

ORD 기록
ord-3149f9ef5e4f447b8689df793a48b5c5
출처 데이터셋
uspto-grants-1997_09
특허 번호
US05670512

반응 노트

불러오는 중…