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Acrylamide → 8-chloro-1,4,5,6-tetrahydrobenzo[f]quinolin-3(2H)-one

HRID 1639356
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반응식

HRID 1639356 반응식
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([N:12]1[CH2:16][CH2:15][CH2:14]C1)[CH2:6][CH2:5]2.C(N)(=[O:20])C=C>C(O)C>[Cl:1][C:2]1[CH:11]=[CH:10][C:9]2[C:8]3[CH2:14][CH2:15][C:16](=[O:20])[NH:12][C:7]=3[CH2:6][CH2:5][C:4]=2[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6579AcrylamideHCID 10444008Pyrrolidine, 1-(6-chloro-3,4-dihydro-2-naphthalenyl)-

생성물 1

HCID 104665398-chloro-1,4,5,6-tetrahydrobenzo[f]quinolin-3(2H)-one

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

701 g (3 mol) of 1-(6-chloro-3,4-dihydro-2-naphthyl)-pyrrolidine and 640 g (19 mol) of acrylamide in 7 ml of ethanol are boiled under reflux for 3 days with the addition of 70 g of Amberlite IR200. The separated solid is removed by filtration, extractively crystallized with dioxane and there is obtained 8-chloro-1,4,5,6-tetrahydrobenzo[f]-quinolin-3(2H)-one with melting point 228°-230° C.

후처리

  1. temperatureunder reflux for 3 days with the addition of 70 g of Amberlite IR200
  2. customThe separated solid is removed by filtration
  3. customextractively crystallized with dioxane

출처 및 근거

ORD 기록
ord-cc85e2db7142473394fe502977c273ba
출처 데이터셋
uspto-grants-1989_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04883815

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