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Hydrochloric Acid → Triazamate acid

HRID 1252157
ノート
印刷プレビュー

反応式

HRID 1252157 の反応式
[CH3:1][N:2]([CH3:21])[C:3]([N:5]1[C:9]([S:10][CH2:11][C:12]([O:14]CC)=[O:13])=[N:8][C:7]([C:17]([CH3:20])([CH3:19])[CH3:18])=[N:6]1)=[O:4].Cl>C1COCC1>[CH3:1][N:2]([CH3:21])[C:3]([N:5]1[C:9]([S:10][CH2:11][C:12]([OH:14])=[O:13])=[N:8][C:7]([C:17]([CH3:19])([CH3:18])[CH3:20])=[N:6]1)=[O:4]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 313Hydrochloric AcidHCID 86306Triazamate

生成物 1

HCID 14299898Triazamate acid

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
20 °C

実験手順

To 1.2 g of 1-dimethylcarbamoyl-3-t-butyl-5-carboethoxymethylthio-1H-1,2,4-triazole (the compound of Example 2) in 20 ml of THF was added 4 ml of 12M HCl. After stirring for 48 h at 20° C. the reaction mixture was partitioned between ether and water, the ether layer was extracted with dilute NaOH and the resulting aqueous layer was acidified and extracted with fresh ether. The resulting ether layer was dried over magnesium sulfate, filtered and evaporated under vacuum to yield 1-dimethylcarbamoyl-3-t-butyl-5-carboxymethylthio-1H-1,2,4-triazole as an oil.

後処理

  1. customwas partitioned between ether and water
  2. extractionthe ether layer was extracted with dilute NaOH
  3. extractionextracted with fresh ether
  4. dry with materialThe resulting ether layer was dried over magnesium sulfate
  5. filtrationfiltered
  6. customevaporated under vacuum

出典と根拠

ORDレコード
ord-1d7b0b845d974955b99d01aaaf83b577
出典データセット
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04742072

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート