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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Toluene → Phenol, 4-[(phenylimino)methyl]-

HRID 278287
ノート
印刷プレビュー

反応式

HRID 278287 の反応式
[OH:1]C1C=CC=CC=1C=O.[NH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.[C:17]1([CH3:23])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[OH:1][C:20]1[CH:21]=[CH:22][C:17]([CH:23]=[N:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:18][CH:19]=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 3

HCID 1140TolueneHCID 6115Aniline2 回HCID 6998Salicylaldehyde

生成物 1

HCID 74319Phenol, 4-[(phenylimino)methyl]-収率 94%

実験手順

A solution of hydroxy benzaldehyde (5.00 g, 41 mmol) in toluene (200 cm3) was heated to 109° C. before aniline (1.86 g, 20 mmol) was added under nitrogen. The mixture was then allowed to cool, forming a yellow solid after 30 minutes. The reaction was continued with the further addition of aniline (1.86 g, 20 mmol). Dean and Stark apparatus was used to collect water (0.6 cm3). Reflux continued for a further 5 hours by which time 0.7 cm3 of water had collected. After cooling the mixture, a thick crystalline mass was formed which was filtered and dried under vacuum at 90° C. to give 4-hydroxybenzylidene-aniline (7.3 g, 94%) as pale cream crystals.

後処理

  1. additionwas added under nitrogen
  2. temperatureto cool
  3. customforming a yellow solid after 30 minutes
  4. customto collect water (0.6 cm3)
  5. temperatureReflux
  6. customhad collected
  7. temperatureAfter cooling the mixture
  8. customa thick crystalline mass was formed which
  9. filtrationwas filtered
  10. customdried under vacuum at 90° C.

出典と根拠

ORDレコード
ord-0489a8bb32924320949f9d9d01e77ca7
出典データセット
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06359056B1

反応ノート

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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