1,2-Dimethoxyethane → 2-[2-(4-Tetradecenylamino)phenyl]oxazoline

HRID 325574

反応式

HRID 325574 の反応式
Br.Br[CH2:3][CH2:4][NH2:5].COCCOC.Cl.[CH2:13]([NH:27][C:28]1[CH:36]=[CH:35][CH:34]=[CH:33][C:29]=1[C:30](Cl)=[O:31])[CH2:14][CH2:15][CH:16]=[CH:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]>CN(C)C1C=CN=CC=1.C(N(CC)CC)C>[CH2:13]([NH:27][C:28]1[CH:36]=[CH:35][CH:34]=[CH:33][C:29]=1[C:30]1[O:31][CH2:3][CH2:4][N:5]=1)[CH2:14][CH2:15][CH:16]=[CH:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]

参加物

6

実験手順

To a slurry of 15 g. of 2-bromoethylamine hydrobromide in 150 ml. of 1,2-dimethoxyethane are added simultaneously solutions of 31 g. of 2-(4-tetradecenylamino)benzoyl chloride hydrochloride in 60 ml. of 1,2-dimethoxyethane and 50 cc. of triethylamine (dropwise). Upon addition of 0.5 g. of 4-dimethylaminopyridine the mixture is stirred at room temperature overnight. The solution is refluxed for one hour and filtered. The solid is oven dried and partitioned between methylene chloride and water. The layers are separated and the organic phase dried over magnesium sulfate. The organic layer is concentrated and the residue collected and crystallized from cyclohexane and recrystallized from acetonitrile to yield the product.

後処理

  1. additionUpon addition of 0.5 g
  2. temperatureThe solution is refluxed for one hour
  3. filtrationfiltered
  4. customdried
  5. custompartitioned between methylene chloride and water
  6. customThe layers are separated
  7. dry with materialthe organic phase dried over magnesium sulfate
  8. concentrationThe organic layer is concentrated
  9. customthe residue collected
  10. customcrystallized from cyclohexane
  11. customrecrystallized from acetonitrile
  12. customto yield the product

出典と根拠

ORDレコード
ord-74a655b02ddc4fdba4778b24155f1922
出典データセット
uspto-grants-1984_04
特許番号
US04440940

関連ノート

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