Ammonium Chloride → 1-Methylpiperidine-4-carbaldehyde

HRID 845226ノート

反応式

HRID 845226 の反応式
[CH3:1][N:2]1[CH2:11][CH2:10][CH:5]([C:6](OC)=[O:7])[CH2:4][CH2:3]1.[H-].C([Al+]CC(C)C)C(C)C.[Cl-].[NH4+].C(=O)(O)[O-].[Na+]>CCCCCC>[CH3:1][N:2]1[CH2:11][CH2:10][CH:5]([CH:6]=[O:7])[CH2:4][CH2:3]1

参加物

6

実験手順

To a deep cold (below -70° C.) solution of methyl 1-methylisonipecotate (15.7 g. 0.1 mol) in 500 mL of hexane was added, dropwise over 1 hr, 100 mL of 1N diisobutylaluminum hydride (DIBAL-H) in hexane. The solution was stirred for 1.5 h, and 20 mL of saturated aqueous ammonium chloride was very slowly added. The reaction mixture was gradually allowed to come to ambient temperature and stirring was continued for an additional hour. To the reaction mixture was added 10 mL of saturated aqueous sodium bicarbonate and the organic layer was decanted. The aqueous layer was extracted with methylene chloride (200 mL×3) and then with ether (200 mL×3). The combined extracts were dried with magnesium sulfate and evaporated to give 10 g (79%) of a pale yellow oil (crude). The crude aldehyde was used for further reaction without purification.

後処理

  1. customto come to ambient temperature
  2. stirringstirring
  3. waitwas continued for an additional hour
  4. customthe organic layer was decanted
  5. extractionThe aqueous layer was extracted with methylene chloride (200 mL×3)
  6. dry with materialThe combined extracts were dried with magnesium sulfate
  7. customevaporated

出典と根拠

ORDレコード
ord-5e6011a20403486abadfb5db6ff62bf1
出典データセット
uspto-grants-1988_07
特許番号
US04757079

反応ノート

読み込み中…