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Triethylamine → HCID 23462043、化合物

HRID 2286700
ノート
印刷プレビュー

反応式

HRID 2286700 の反応式
[OH:1][CH2:2][C:3]1[CH:8]=[N:7][C:6]([CH3:9])=[CH:5][N:4]=1.C(N(CC)CC)C.[C:17](Cl)(=[O:22])[C:18]([CH3:21])([CH3:20])[CH3:19]>C1C=CC=CC=1>[C:17]([O:1][CH2:2][C:3]1[CH:8]=[N:7][C:6]([CH3:9])=[CH:5][N:4]=1)(=[O:22])[C:18]([CH3:21])([CH3:20])[CH3:19]
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 8471TriethylamineHCID 62493Pivaloyl chlorideHCID 5800615-Methyl-2-pyrazinemethanol

生成物 1

HCID 23462043HCID 23462043、化合物収率 71.5%

試薬・触媒・溶媒 1

HCID 241Benzene溶媒2 回

実験手順

To a solution of 2-hydroxymethyl-5-methylpyrazine (6.2 g) and triethylamine (6.4 ml) in anhydrous benzene (150 ml) dropwise addition was made of a solution of pivaloyl chloride (6.15 ml) in anhydrous benzene (50 ml). The solution was maintained at boiling for 7 hours, the solvent was then evaporated and the residue treated with acetone. After filtration of the insoluble solid, the filtrate was evaporated to dryness and the residue re-dissolved in chloroform. The chloroform solution was first dehydrated and then evaporated to dryness, obtaining 7 g (71.5%) of 5-methyl-2-pyrazinylmethyl pivalate, b.p.=74° C./0.1 mmHg.

後処理

  1. temperatureThe solution was maintained
  2. customthe solvent was then evaporated
  3. additionthe residue treated with acetone
  4. filtrationAfter filtration of the insoluble solid
  5. customthe filtrate was evaporated to dryness
  6. dissolutionthe residue re-dissolved in chloroform
  7. customevaporated to dryness

出典と根拠

ORDレコード
ord-d264a38a797541b085380ef383a4575e
出典データセット
uspto-grants-1981_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04267327

反応ノート

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