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Sodium hydride → 5-(N,N-Dibenzylglycyl)-2-[2-(2-ethoxyethoxy)ethoxy] benzamide

HRID 1974215
ノート
印刷プレビュー

反応式

HRID 1974215 の反応式
[CH2:1]([N:8]([CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)[CH2:9][C:10]([C:12]1[CH:20]=[C:16]([C:17]([NH2:19])=[O:18])[C:15]([OH:21])=[CH:14][CH:13]=1)=[O:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Na+].C1(C)C=CC(S(O[CH2:41][CH2:42][O:43][CH2:44][CH2:45][O:46][CH2:47][CH3:48])(=O)=O)=CC=1>CN(C)C=O>[CH2:22]([N:8]([CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)[CH2:9][C:10]([C:12]1[CH:13]=[CH:14][C:15]([O:21][CH2:41][CH2:42][O:43][CH2:44][CH2:45][O:46][CH2:47][CH3:48])=[C:16]([CH:20]=1)[C:17]([NH2:19])=[O:18])=[O:11])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1
参加物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 24758Sodium hydrideHCID 1217275-((Bis(benzyl)amino)acetyl)salicylamideHCID 41182322-(2-Ethoxyethoxy)ethyl 4-methylbenzene-1-sulfonate

生成物 1

HCID 214888835-(N,N-Dibenzylglycyl)-2-[2-(2-ethoxyethoxy)ethoxy] benzamide収率 93.1%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

実験手順

A solution of 5-(N,N-dibenzylglycyl)salicylamide (10 g.) in dimethylformamide (75 ml) was added dropwise to a stirred suspension of sodium hydride (0.875 g) in dimethylformamide (25 ml). 2-(2 -Ethoxyethoxy)ethyl p-toluenesulphonate (12.75 g) was then added and the solution heated at 100° for 2 hours. The solvent was evaporated to give a yellow oily solid which was partitioned between ethyl acetate and water. The ethyl acetate layer was dried (MgSO4), concentrated to 30 ml and chromatographed on alumina (60 g.). The column was eluted with ethyl acetate (100 ml portions). The first fraction was discarded and the subsequent four fractions yielded an oil (12.2 g) which crystallised from ethanol to give the ether as colourless plates (5.8 g) m.p. 91.5°-92.5°. Recrystallisation of a sample raised the m.p. to 92.5°-94°.

後処理

  1. temperaturethe solution heated at 100° for 2 hours
  2. customThe solvent was evaporated
  3. customto give a yellow oily solid which
  4. customwas partitioned between ethyl acetate and water
  5. dry with materialThe ethyl acetate layer was dried (MgSO4)
  6. concentrationconcentrated to 30 ml
  7. customchromatographed on alumina (60 g.)
  8. washThe column was eluted with ethyl acetate (100 ml portions)

出典と根拠

ORDレコード
ord-58455cdef3c54df68bcdce7a881218df
出典データセット
uspto-grants-1976_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04000192

反応ノート

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