Ethyl chloroformate → 4-(p-FLUOROBENZOYL)-4-HYDROXYPIPERIDINE HYDROCHLORIDE

HRID 2397471ノート

反応式

HRID 2397471 の反応式
C([O:4][C:5]1([C:12](=[O:20])[C:13]2[CH:18]=[CH:17][C:16]([F:19])=[CH:15][CH:14]=2)[CH2:10][CH2:9][N:8](C)[CH2:7][CH2:6]1)(=O)C.[Cl:21]C(OCC)=O>C1C=CC=CC=1>[ClH:21].[F:19][C:16]1[CH:17]=[CH:18][C:13]([C:12]([C:5]2([OH:4])[CH2:10][CH2:9][NH:8][CH2:7][CH2:6]2)=[O:20])=[CH:14][CH:15]=1

参加物

4

反応物 2

HCID 10928Ethyl chloroformateHCID 21438446HCID 21438446、化合物

生成物 1

HCID 214351194-(p-FLUOROBENZOYL)-4-HYDROXYPIPERIDINE HYDROCHLORIDE

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

To 27.9 grams (0.1 mole) of 4-acetoxy-4-(p-fluorobenzoyl)-1-methylpiperidine in 200 ml. of benzene was added 27.1 (0.25 mole) of ethyl chloroformate. The mixture was refluxed for 48 hours. The mixture was extracted with H2O, the organic solution was dried (MgSO4) and filtered. The filtrate was concentrated. To the resulting oil was added 250 ml. of 6 Normal HCl and the mixture was refluxed for seventy-two hours. Most of the water was removed under reduced pressure. Ethanol was added and the solution cooled. The solid which precipitated was collected by filtration and recrystallized from ethanol giving eighteen grams of 4-(p-fluorobenzoyl)-4-hydroxypiperidine hydrochloride. Melting point 241°-243° C.

後処理

  1. temperatureThe mixture was refluxed for 48 hours
  2. extractionThe mixture was extracted with H2O
  3. dry with materialthe organic solution was dried (MgSO4)
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated
  6. additionTo the resulting oil was added 250 ml
  7. temperatureof 6 Normal HCl and the mixture was refluxed for seventy-two hours
  8. customMost of the water was removed under reduced pressure
  9. additionEthanol was added
  10. temperaturethe solution cooled
  11. customThe solid which precipitated
  12. filtrationwas collected by filtration
  13. customrecrystallized from ethanol giving eighteen grams of 4-(p-fluorobenzoyl)-4-hydroxypiperidine hydrochloride

出典と根拠

ORDレコード
ord-6c5d9db3dbc44eb38243c8bfa9e9174d
出典データセット
uspto-grants-1977_05
特許番号
US04021564

反応ノート

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