Sodium borohydride → 4-Phenyl-4-piperidinocyclohexanol

HRID 1464238ノート

反応式

HRID 1464238 の反応式
[C:1]1([C:7]2([N:14]3[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]3)[CH2:12][CH2:11][C:10](=[O:13])[CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[BH4-].[Na+]>CO>[C:1]1([C:7]2([N:14]3[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]3)[CH2:8][CH2:9][CH:10]([OH:13])[CH2:11][CH2:12]2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

参加物

4

反応物 2

HCID 4311764Sodium borohydrideHCID 133067564-Phenyl-4-piperidinocyclohexanone

生成物 1

HCID 1621714-Phenyl-4-piperidinocyclohexanol収率 85%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

The cyclohexanone derivative of Example 3 (1 g; 3.9 mmole) was dissolved in 50 ml of methanol inside a three-necked round bottom flask equipped with a condenser. 0.5 g of sodium borohydride was added portionwise to this solution. After addition, the mixture was stirred at room temperature for 2 hours. The methanol was removed under reduced pressure to give a solid residue. The solid residue was extracted with ethyl acetate. The ethyl acetate extracts were combined and washed once with water and dried over anhydrous sodium sulfate. Ethyl acetate was removed to give a solid material. The solid was recrystallized from hexane/ether (1:1; v/v) to give the desired cyclohexanol derivative as a white crystalline solid (0.89 g; 85% yield).

後処理

  1. customequipped with a condenser
  2. additionAfter addition
  3. customThe methanol was removed under reduced pressure
  4. customto give a solid residue
  5. extractionThe solid residue was extracted with ethyl acetate
  6. washwashed once with water
  7. dry with materialdried over anhydrous sodium sulfate
  8. customEthyl acetate was removed
  9. customto give a solid material
  10. customThe solid was recrystallized from hexane/ether (1:1; v/v)

出典と根拠

ORDレコード
ord-588b0926c9a84d7c9f5b6440cebad53f
出典データセット
uspto-grants-1994_04
特許番号
US05304479

反応ノート

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