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Methyl Isocyanate → 5-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]-2,4-dihydro-4-methyl-3H-1,2,4-triazol-3-one

HRID 466051
ノート
印刷プレビュー

反応式

HRID 466051 の反応式
[CH3:1][N:2]=[C:3]=[O:4].[CH3:5][C:6]([C:9]1[CH:10]=[C:11]([CH:16]=[C:17]([C:20]([CH3:23])([CH3:22])[CH3:21])[C:18]=1[OH:19])[C:12]([NH:14][NH2:15])=O)([CH3:8])[CH3:7].[OH-].[Na+]>C(O)C>[CH3:5][C:6]([C:9]1[CH:10]=[C:11]([C:12]2[N:2]([CH3:1])[C:3](=[O:4])[NH:15][N:14]=2)[CH:16]=[C:17]([C:20]([CH3:23])([CH3:22])[CH3:21])[C:18]=1[OH:19])([CH3:8])[CH3:7]
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 12228Methyl IsocyanateHCID 14798Sodium HydroxideHCID 104229343,5-Di-tert-butyl-4-hydroxybenzohydrazide

生成物 1

HCID 1355181725-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]-2,4-dihydro-4-methyl-3H-1,2,4-triazol-3-one収率 30%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Methyl isocyanate (1.02 g, 18 mmol) is added dropwise to a solution of the 3,5-bis(1,1-dimethylethyl)-4-hydroxybenzoic acid, hydrazide (2.35 g, 8.9 mmol) in absolute ethanol (100 ml). The reaction mixture is stirred at room temperature, concentrated, and poured into ice water. The precipitate (1.2 g) is collected by filtration and dissolved in two equivalents of 1N NaOH. The reaction mixture is refluxed for three hours, and then is cooled and neutralized. The product is extracted into ethyl acetate. Pure 5-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]-2,4-dihydro-4-methyl-3H-1,2,4-triazol-3-one (0.8 g, 30%) is obtained by recrystallization from methanol, mp 308°-312° C.

後処理

  1. concentrationconcentrated
  2. additionpoured into ice water
  3. filtrationThe precipitate (1.2 g) is collected by filtration
  4. temperatureThe reaction mixture is refluxed for three hours
  5. temperatureis cooled
  6. extractionThe product is extracted into ethyl acetate

出典と根拠

ORDレコード
ord-869fd573e8e845559aa86f1e8f73c7db
出典データセット
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05155122

反応ノート

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