Bromide ion → Benzyl 4-methylidenepiperidine-1-carboxylate

HRID 2300143

反応式

HRID 2300143 の反応式
[Br-].[C:2](O[K])([CH3:5])([CH3:4])[CH3:3].O=C1C[CH2:13][N:12]([C:15]([O:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[O:16])[CH2:11]C1>O1CCCC1>[CH2:3]=[C:2]1[CH2:5][CH2:11][N:12]([C:15]([O:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[O:16])[CH2:13][CH2:4]1

参加物

5

反応物 3

HCID 259Bromide ionHCID 643496Benzyl 4-oxopiperidine-1-carboxylateHCID 178418922HCID 178418922、化合物

生成物 1

HCID 15519136Benzyl 4-methylidenepiperidine-1-carboxylate収率 159.7%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

51.1 g of methyltoluphenylphosphonium bromide was added to a mixture of 16.1 g tert-butoxy potassium and 500 ml tetrahydrofuran, and then stirred for 1 hr and 20 min at room temperature. 16.1 g of benzyl 4-oxo-1-piperidinecarboxylate was added thereto, and the mixture was stirred for 2 hr and 40 min at room temperature. The reaction solution was evaporated, diethyl ether was added thereto, and then filtered through Celite. The filtrate was washed with water and brine, dried over anhydrous magnesium sulfate, and then filtered. The filtrate was evaporated, and the resulting residue was subjected to silica gel column chromatography to give 25.5 g of benzyl 4-methylene-1-piperidinecarboxylate.

後処理

  1. stirringthe mixture was stirred for 2 hr and 40 min at room temperature
  2. customThe reaction solution was evaporated
  3. additiondiethyl ether was added
  4. filtrationfiltered through Celite
  5. washThe filtrate was washed with water and brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. customThe filtrate was evaporated

出典と根拠

ORDレコード
ord-38d2746c90ab49d69f41b89142ceb2ac
出典データセット
uspto-grants-2002_12
特許番号
US06498159B1

関連ノート

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