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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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3-Pyridinecarboxaldehyde → Pyridine, 3-(2,2-dibromoethenyl)-

HRID 1760
ノート
印刷プレビュー

反応式

HRID 1760 の反応式
[Br:1][C:2]([Br:5])(Br)Br.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[N:25]1[CH:30]=[CH:29][CH:28]=[C:27]([CH:31]=O)[CH:26]=1>C(Cl)Cl>[Br:1][C:2]([Br:5])=[CH:31][C:27]1[CH:26]=[N:25][CH:30]=[CH:29][CH:28]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 103713-PyridinecarboxaldehydeHCID 11205Carbon tetrabromideHCID 11776Triphenylphosphine

生成物 1

HCID 11334526Pyridine, 3-(2,2-dibromoethenyl)-収率 70%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

Tetrabromomethane (24.82 g, 0.747 mole) and triphenylphosphine (39.17 g, 0.149 mole) were stirred together in dry methylene chloride (100 mL) for 5 min. at 0° C. under a nitrogen atmosphere. To this mixture was added dropwise pyridine 3-carboxaldehyde (4 g, 0.0373 mole). The solution was then stirred for 45 min. at ambient temperature. The reaction mixture was extracted with aqueous 6N hydrochloric acid (3×25 mL), the aqueous layer basified with solid sodium bicarbonate to pH 8-9 and extracted with chloroform (4×25 mL). The combined organic liquours were dried over anhydrous sodium sulfate, filtered and concentrated on a rotary evaporator to give a dark colored syrup. The crude product was chromatographed on silica gel (70-230 mesh) with chloroform:methanol (95:5) as eluant, to afford a light yellow solid (5.0 g, 70%) which rapidly turned dark on standing.

後処理

  1. extractionThe reaction mixture was extracted with aqueous 6N hydrochloric acid (3×25 mL)
  2. extractionextracted with chloroform (4×25 mL)
  3. dry with materialThe combined organic liquours were dried over anhydrous sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated on a rotary evaporator
  6. customto give a dark colored syrup
  7. customThe crude product was chromatographed on silica gel (70-230 mesh) with chloroform:methanol (95:5) as eluant

出典と根拠

ORDレコード
ord-b463cdcceaba4202b2513724f75023cf
出典データセット
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05726316

反応ノート

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