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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Bromobenzene → HCID 12876530、化合物

HRID 1395656
ノート
印刷プレビュー

反応式

HRID 1395656 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 7961BromobenzeneHCID 3028194LithiumHCID 10932403HCID 10932403、化合物HCID 178506676HCID 178506676、化合物

生成物 1

HCID 12876530HCID 12876530、化合物

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 3283
Diethyl Ether
溶媒
2 回

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-a3dc864c84054385b58ff0743a490607
出典データセット
uspto-grants-1980_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04205074

反応ノート

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