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Bromobenzene → HCID 12876530, 화합물

HRID 1395656
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HRID 1395656 반응식
[C:1]1([Li])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Li].Br[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.C(O[C:19]([CH:21]1[CH:29]2[N:24]([CH2:25][CH2:26][CH2:27][CH2:28]2)[CH2:23][CH2:22]1)=O)C>O.CCOCC>[C:1]1([C:19]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[C:21]2[CH:29]3[N:24]([CH2:25][CH2:26][CH2:27][CH2:28]3)[CH2:23][CH2:22]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 7961BromobenzeneHCID 3028194LithiumHCID 10932403HCID 10932403, 화합물HCID 178506676HCID 178506676, 화합물

생성물 1

HCID 12876530HCID 12876530, 화합물

시약·촉매·용매 2

HCID 962Water용매HCID 3283
Diethyl Ether
용매
2회

실험 절차

To a phenyl lithium solution prepared by dissolving 0.51 g. of metallic lithium and 6.32 g. of bromobenzene in 50 ml. of absolute ether, was dropwise added a solution of 2.40 g. of 1-ethoxycarbonylindolizidine in 20 ml. of absolute ether under ice cooling. After refluxing for about 10 mins., water was dropwise added thereto, followed by extraction with ether. The ethereal layer was further extracted with dil. hydrochloric acid. The aqueous layer was rendered alkaline with an aq. sodium hydroxide solution and then extracted with ether. The ethereal layer was washed with water and dried. After removing the solvent by distillation, 3.58 g. of light yellow viscous substance was obtained.

후처리

  1. dissolutionby dissolving 0.51 g
  2. temperatureAfter refluxing for about 10 mins
  3. extractionfollowed by extraction with ether
  4. extractionThe ethereal layer was further extracted with dil. hydrochloric acid
  5. extractionextracted with ether
  6. washThe ethereal layer was washed with water
  7. customdried
  8. customAfter removing the solvent
  9. distillationby distillation, 3.58 g
  10. customof light yellow viscous substance was obtained

출처 및 근거

ORD 기록
ord-a3dc864c84054385b58ff0743a490607
출처 데이터셋
uspto-grants-1980_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04205074

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