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Hydrochloric Acid → HCID 178423709、化合物

HRID 651261
ノート
印刷プレビュー

反応式

HRID 651261 の反応式
[C:1]([C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]1[CH:14]=[CH:13][C:12]([CH3:15])=[CH:11][CH:10]=1)#[N:2].[NH2:16][NH2:17].[N:18]([O-])=O.[Na+].Cl>C(O)C>[NH:16]1[C:1]([C:3]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=2[C:9]2[CH:10]=[CH:11][C:12]([CH3:15])=[CH:13][CH:14]=2)=[N:2][N:18]=[N:17]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 4

HCID 313Hydrochloric AcidHCID 9321HydrazineHCID 1455122-Cyano-4'-methylbiphenylHCID 23668193Sodium Nitrite

生成物 1

HCID 178423709HCID 178423709、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

First, 26.9 mmol of 2-cyano-4′-methyl-1,1′-biphenyl was dissolved in 150 ml of ethanol, and 270 mmol of hydrazine and 77.7 mmol of 28% methylate were added thereto, followed by keeping at 50° C. for 48 hours. The reaction mixture was concentrated under reduced pressure. The residue was dissolved in 100 ml of ethanol, and 55 mmol of sodium nitrite and 110 mmol of concentrated hydrochloric acid were added to the solution at 0° C. After keeping at 0-5° C. for 2 hours, the reaction mixture was concentrated to give 2-(tetrazol-5-yl)-4′-methyl-1,1′-biphenyl. Yield, 46%

後処理

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. dissolutionThe residue was dissolved in 100 ml of ethanol
  3. waitAfter keeping at 0-5° C. for 2 hours
  4. concentrationthe reaction mixture was concentrated

出典と根拠

ORDレコード
ord-0bd65599add04984b119975b76742617
出典データセット
uspto-grants-2001_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06277998B1

反応ノート

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