Ethylene Glycol → 1-Acetyl-4-[2-(4-fluorophenyl)-1,3-dioxolan-2-yl]piperidine

HRID 1975039ノート

反応式

HRID 1975039 の反応式
[C:1]([N:4]1[CH2:9][CH2:8][CH:7]([C:10](=[O:18])[C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)[CH2:6][CH2:5]1)(=[O:3])[CH3:2].[CH2:19](O)[CH2:20][OH:21].CC1C=CC(S(O)(=O)=O)=CC=1.C1C=CC=CC=1>O>[C:1]([N:4]1[CH2:9][CH2:8][CH:7]([C:10]2([C:11]3[CH:12]=[CH:13][C:14]([F:17])=[CH:15][CH:16]=3)[O:21][CH2:20][CH2:19][O:18]2)[CH2:6][CH2:5]1)(=[O:3])[CH3:2]

参加物

6

反応物 4

HCID 174Ethylene GlycolHCID 241BenzeneHCID 6101p-Toluenesulfonic acidHCID 1172571-Acetyl-4-(4-fluorobenzoyl)piperidine

生成物 1

HCID 191009161-Acetyl-4-[2-(4-fluorophenyl)-1,3-dioxolan-2-yl]piperidine収率 56.8%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A mixture of 74.7 parts of 1-acetyl-4-(4-fluorobenzoyl)piperidine, 46.5 parts of 1,2-ethanediol, 3 parts of 4-methylbenzenesulfonic acid and 810 parts of benzene was stirred for 108 hours at reflux temperature using a water separator. After cooling, the reaction mixture was washed successively with 250 parts of water, 22.5 parts of ammonium hydroxide and 250 parts of water. The organic layer was dried, filtered and evaporated. The residue was purified by column chromatography (silica gel; CHCl3 /CH3COCH3 50:50). The eluent of the desired fraction was evaporated, yielding 50 parts (56.8%) of 1-acetyl-4-[2-(4-fluorophenyl)-1,3-dioxolan-2-yl]piperidine (interm. 45).

後処理

  1. temperatureat reflux temperature
  2. temperatureAfter cooling
  3. washthe reaction mixture was washed successively with 250 parts of water, 22.5 parts of ammonium hydroxide and 250 parts of water
  4. customThe organic layer was dried
  5. filtrationfiltered
  6. customevaporated
  7. customThe residue was purified by column chromatography (silica gel; CHCl3 /CH3COCH3 50:50)
  8. customThe eluent of the desired fraction was evaporated

出典と根拠

ORDレコード
ord-2ea73cc2d0e74d2aaeb0c5b1c866b63f
出典データセット
uspto-grants-1994_02
特許番号
US05284854

反応ノート

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