Potassium Carbonate → 1-(2-Methoxyethyl)piperidine-4-carbaldehyde

HRID 1795155ノート

反応式

HRID 1795155 の反応式
C([O:3][C:4]([CH:6]1[CH2:11][CH2:10][N:9]([CH2:12][CH2:13][O:14][CH3:15])[CH2:8][CH2:7]1)=O)C.N1CCC(C(OCC)=O)CC1.C(=O)([O-])[O-].[K+].[K+].COCCBr>C(O)C>[CH3:15][O:14][CH2:13][CH2:12][N:9]1[CH2:10][CH2:11][CH:6]([CH:4]=[O:3])[CH2:7][CH2:8]1

参加物

6

実験手順

1-(2-Methoxyethyl)-piperidine-4-carboxylic acid ethyl ester A solution of ethyl isonipecotate (26 g, 166 mmol) in ethanol (150 ml) was treated with potassium carbonate (41 g, 297 mmol) and 2-bromoethyl methyl ether (25 g, 179 mmol). The reaction mixture was heated to reflex for 24 hours, cooled and then filtered. The filtrate was concentrated in vacuo to yield the title compound (32.76 g, 92%); MS(ES+) m/e 216 [M+H]+. Step 2. 1-(2-Methoxyethyl)-piperidine-4-carbaldehyde Diisobutylaluminium hydride (10.2 ml, 1M solution in THF) was added to a solution of the product of Step 1 (2.0 g, 9.3 mmol) in toluene (40 ml) over a period of 1 hour at −78° C. The reaction was stirred at −78° C. for 1 hour and then quenched with methanol (5 ml) and aqueous ammonium acetate solution (5 ml). The mixture was stirred for 1 hour and then filtered through celite. The filtrate was concentrated in vacuo to yield the title compound (1.1 g, 69%); MS(ES+) m/e 172 [M+H]+.

後処理

  1. temperatureThe reaction mixture was heated
  2. temperaturecooled
  3. filtrationfiltered
  4. concentrationThe filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-68b2c657a3274e07bac91e86fd8b822a
出典データセット
uspto-grants-2006_04
特許番号
US07026336B1

反応ノート

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