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Ammonium → HCID 18977005、化合物

HRID 2393724
ノート
印刷プレビュー

反応式

HRID 2393724 の反応式
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[N:8]([CH2:11][CH2:12][CH2:13][CH2:14][N:15]=[N+:16]=[N-:17])=[N+:9]=[N-:10].[NH4+:18]>CCCCC.CCCCCC>[N:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[NH:10][N:9]=[N:8][CH2:11][CH2:12][CH2:13][CH2:14][N:15]=[N:16][NH:17][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:18]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 223AmmoniumHCID 79732-BromopyridineHCID 136209641,4-Diazidobutane

生成物 1

HCID 18977005HCID 18977005、化合物

試薬・触媒・溶媒 2

HCID 8003Pentane溶媒2 回HCID 8058Hexane溶媒

実験手順

A solution of 3.95 g (25 mmoles) of 2-bromopyridine in 20 ml of dry pentane was added dropwise to 10 ml. of 2.5M butylithium in hexane at -78° C. To the resulting yellow slurry was added dropwise with stirring 1.75 g (12.5 mmoles) of 1,4-diazidobutane in 10 ml. of pentane. Stirring was continued for 2 hr. at -78° and then the reaction mixture was allowed to warm to room temperature. The reaction mixture was treated with 60 ml. of ammonium buffer which caused a precipitate to appear after the reaction was cooled to -78° C. The solid was filtered off. It was poorly soluble in common solvents such as halomethanes, acetone, methanol and water. It was sparingly soluble in dimethylsulfoxide. The yield was 2.3 g., m.p. 133-136. Spectroscopic data were consistent with the structure.

後処理

  1. customat -78° C
  2. additionTo the resulting yellow slurry was added dropwise
  3. customat -78°
  4. additionThe reaction mixture was treated with 60 ml
  5. temperaturewas cooled to -78° C
  6. filtrationThe solid was filtered off

出典と根拠

ORDレコード
ord-2593938d6c904d25a07ee2dfcc429eb7
出典データセット
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05808038

反応ノート

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