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Nitric Acid → 4-Propyl-4H-1,2,4-triazole-3-methanol

HRID 856646
ノート
印刷プレビュー

反応式

HRID 856646 の反応式
[N+]([O-])(O)=O.N([O-])=O.[Na+].[OH:9][CH2:10][C:11]1[N:15]([CH2:16][CH2:17][CH3:18])[C:14](S)=[N:13][N:12]=1.C(=O)([O-])[O-].[Na+].[Na+]>O>[OH:9][CH2:10][C:11]1[N:15]([CH2:16][CH2:17][CH3:18])[CH:14]=[N:13][N:12]=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 944Nitric AcidHCID 10340Sodium CarbonateHCID 23668193Sodium NitriteHCID 178456617HCID 178456617、化合物

生成物 1

HCID 229386294-Propyl-4H-1,2,4-triazole-3-methanol収率 73%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a mixture of 90% nitric acid (18 ml) and water (26 ml) was added sodium nitrite (0.07 g) and then 3-hydroxymethyl-5-mercapto-4-propyl-4H-1,2,4-triazole (10 g) was slowly added for 0.5 hours at 45° C. After cooling to room temperature, and sodium carbonate was slowly added thereto to adjust pH to 7 at 0° C. The reaction mixture was concentrated under reduced pressure, methanol was added to the residue, and the precipitates were removed by filtration. The mixture was concentrated under reduced pressure, dichloromethane was added to the residue, the precipitates were removed by filtration, and the filtrate was concentrated to give 3-hydroxymethyl-4-propyl-4H-1,2,4-triazole (5.95 g) as a crude product.

後処理

  1. customto adjust pH to 7 at 0° C
  2. concentrationThe reaction mixture was concentrated under reduced pressure, methanol
  3. additionwas added to the residue
  4. customthe precipitates were removed by filtration
  5. concentrationThe mixture was concentrated under reduced pressure, dichloromethane
  6. additionwas added to the residue
  7. customthe precipitates were removed by filtration
  8. concentrationthe filtrate was concentrated

出典と根拠

ORDレコード
ord-d6531465c312481f9a67b11d79fb6e36
出典データセット
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07262185B2

反応ノート

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