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(2-Methyl-1H-benzimidazol-4-yl)methanol → 2-methyl-1H-benzo[d]imidazole-4-carbaldehyde

HRID 1723111
ノート
印刷プレビュー

反応式

HRID 1723111 の反応式
[CH3:1][C:2]1[NH:6][C:5]2[CH:7]=[CH:8][CH:9]=[C:10]([CH2:11][OH:12])[C:4]=2[N:3]=1>[O-2].[Mn+4].[O-2].C(OCC)(=O)C>[CH3:1][C:2]1[NH:6][C:5]2[CH:7]=[CH:8][CH:9]=[C:10]([CH:11]=[O:12])[C:4]=2[N:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 20026664(2-Methyl-1H-benzimidazol-4-yl)methanol

生成物 1

HCID 200266662-methyl-1H-benzo[d]imidazole-4-carbaldehyde収率 35.2%

試薬・触媒・溶媒 2

HCID 178418406HCID 178418406、化合物触媒HCID 8857Ethyl Acetate溶媒

実験手順

(a-3) A mixture of 10 parts of 2-methyl-1H-benzimidazole-4-methanol, 10 parts of manganese(IV) oxide and 180 parts of ethyl acetate was stirred for 19 hours at room temperature. The reaction mixture was filtered over diatomaceous earth and washed with a mixture of ethyl acetate and methanol (80:20 by volume). The filtrate was evaporated and the residue was crystallized from 2-butanone. The product was filtered off and dried, yielding 3.5 parts (35.2%) of 2-methyl-1H-benzimidazole-4-carboxaldehyde (int. 67).

後処理

  1. filtrationThe reaction mixture was filtered over diatomaceous earth
  2. washwashed with a mixture of ethyl acetate and methanol (80:20 by volume)
  3. customThe filtrate was evaporated
  4. customthe residue was crystallized from 2-butanone
  5. filtrationThe product was filtered off
  6. customdried

出典と根拠

ORDレコード
ord-f664c30654984e57bc5880aecc0f5139
出典データセット
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04859684

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート