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Ethyl ketone → HCID 18187644、化合物

HRID 1862709
ノート
印刷プレビュー

反応式

HRID 1862709 の反応式
C(NC(C)C)(C)C.C([Li])CCC.[CH3:13][CH2:14][C:15](=[O:18])[CH2:16][CH3:17].[C:19]([O:23][C:24]([N:26]1[CH2:31][CH2:30][CH:29]([CH:32]=[O:33])[CH2:28][CH2:27]1)=[O:25])([CH3:22])([CH3:21])[CH3:20]>C1COCC1>[C:19]([O:23][C:24]([N:26]1[CH2:31][CH2:30][CH:29]([CH:32]([OH:33])[CH:14]([CH3:13])[C:15](=[O:18])[CH2:16][CH3:17])[CH2:28][CH2:27]1)=[O:25])([CH3:22])([CH3:21])[CH3:20]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 7288Ethyl ketoneHCID 7912DiisopropylamineHCID 1514430tert-Butyl 4-formylpiperidine-1-carboxylateHCID 178418339Butyllithium

生成物 1

HCID 18187644HCID 18187644、化合物収率 85%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
0 °C

実験手順

A solution of diisopropylamine (0.63 mL, 4.5 mmol) in THF (16 mL) at 0° C. was treated with 1.6 M n-butyllithium in sol'n in hexanes (2.8 mL). The resulting solution was stirred at 0° C. for 10 min, then cooled to −78° C. 3-Pentanone (0.41 mL, 4.1 mmol) was added and the resulting mixture was stirred cold for 1 h. A solution of 1-(t-butoxycarbonyl)-4-formylpiperidine (435 mg, 2.05 mmol) (from Step B) in THF (3 mL) was then added. After 15 min, the reaction was quenched with sat'd ammonium chloride (25 mL) and extracted with ether (100 mL). The extract was dried over magnesium sulfate and concentrated. MPLC (Biotage) on a 40S silica cartridge using 4:1 v/v, then 3:2 v/v hexanes/ethyl acetate as the eluent afforded 517 mg (85%) of the title compound.

後処理

  1. temperaturecooled to −78° C
  2. stirringthe resulting mixture was stirred cold for 1 h
  3. waitAfter 15 min
  4. customthe reaction was quenched with sat'd ammonium chloride (25 mL)
  5. extractionextracted with ether (100 mL)
  6. dry with materialThe extract was dried over magnesium sulfate
  7. concentrationconcentrated

出典と根拠

ORDレコード
ord-0c21676921344ab4acaa249cdb294c51
出典データセット
uspto-grants-2003_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06538002B1

反応ノート

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