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Phosphorus oxychloride → 6-[(4-Formylphenyl)(methyl)amino]hexyl acetate

HRID 1199286
ノート
印刷プレビュー

反応式

HRID 1199286 の反応式
P(Cl)(Cl)(Cl)=O.[C:6]([O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][N:16]([CH3:23])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)(=[O:8])[CH3:7].[C:24]([O-])(=[O:26])C.[Na+]>CN(C)C=O>[C:6]([O:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][N:16]([CH3:23])[C:17]1[CH:18]=[CH:19][C:20]([CH:24]=[O:26])=[CH:21][CH:22]=1)(=[O:8])[CH3:7]
参加物反応条件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 24813Phosphorus oxychlorideHCID 517045Sodium AcetateHCID 19697246N-(6-Acetoxyhexyl)-N-methylaniline

生成物 1

HCID 152539796-[(4-Formylphenyl)(methyl)amino]hexyl acetate収率 73%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
5 °C

実験手順

Phosphorous oxychloride (145 g, 0.95 mol) was added dropwise at 5° C. to 280 mL of stirred N,N-dimethylformamide (DMF), and the mixture was stirred at 5° C. for 2 hours. N-(6-Acetoxyhexyl)-N-methylaniline (Example 2, 230 g, 0.93 mol) was added slowly, and the reaction mixture was heated at 90° C. for 3 hours. After cooling, the solution was poured onto 500 g of ice and the resulting mixture was neutralized to pH 5 with sodium acetate. The mixture was extracted with dichloromethane (4×200 mL), the combined extracts were dried (MgSO4), and the solvent was removed at reduced pressure. The brown residue was distilled in vacuo to provide 186 g (73%) of a yellow oil, bp 195° C. (0.15 mm).

後処理

  1. temperaturethe reaction mixture was heated at 90° C. for 3 hours
  2. temperatureAfter cooling
  3. extractionThe mixture was extracted with dichloromethane (4×200 mL)
  4. dry with materialthe combined extracts were dried (MgSO4)
  5. customthe solvent was removed at reduced pressure
  6. distillationThe brown residue was distilled in vacuo

出典と根拠

ORDレコード
ord-3cf62ed54efa4958b9782ef1499031b0
出典データセット
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04900127

反応ノート

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