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Aniline → N-(2,4-dimethoxybenzyl)aniline

HRID 1852415
ノート
印刷プレビュー

反応式

HRID 1852415 の反応式
[CH3:1][O:2][C:3]1[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:4]=1[CH:5]=O.[NH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C1(C)C=CC=CC=1.O.[BH4-].[Na+]>FC(F)(F)C(O)=O.C1(C)C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:4]=1[CH2:5][NH:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 6115AnilineHCID 691752,4-DimethoxybenzaldehydeHCID 4311764Sodium borohydrideHCID 22272177Toluene water

生成物 1

HCID 775299N-(2,4-dimethoxybenzyl)aniline

試薬・触媒・溶媒 2

HCID 6422Trifluoroacetic acid触媒
HCID 1140
Toluene
溶媒

実験手順

Trifluoroaceticacid (10 drops) was added to a solution of 2,4-dimethoxybenzaldehyde (16.62 g, 100 mmol) and aniline (9.31 g, 100 mmol) in toluene (100 mL). The reaction mixture was stirred at reflux temperature and toluene/water was distilled off during 1.5 h. After cooling the reaction mixture was concentrated at reduced pressure and the residue was dissolved in MeOH (200 mL). NaBH4 (2.0 g, 54 mmol) was added in portions during 20 min and the reaction mixture was then stirred for 1 h. The product (22.16 g, 91%) crystallized from the reaction mixture and was isolated by filtration.

後処理

  1. distillationwas distilled off during 1.5 h
  2. temperatureAfter cooling the reaction mixture
  3. concentrationwas concentrated at reduced pressure
  4. dissolutionthe residue was dissolved in MeOH (200 mL)
  5. stirringthe reaction mixture was then stirred for 1 h
  6. customThe product (22.16 g, 91%) crystallized from the reaction mixture
  7. customwas isolated by filtration

出典と根拠

ORDレコード
ord-fb050feb02554d51be6b56241fb812d4
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08962598B2

反応ノート

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