Acetic Acid → HCID 59736092、化合物

HRID 133812

反応式

HRID 133812 の反応式
CC(C)([O-:4])C.[K+].[N+:7]([CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])#[C-:8].[CH2:15]1[C:24](=O)[CH2:23][C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH2:16]1.C(O)(=O)C>O1CCCC1>[C:16]1(=[C:9](/[NH:7][CH:8]=[O:4])\[C:10]([O:12][CH2:13][CH3:14])=[O:11])\[CH2:15][CH2:24][CH2:23][C:22]2[C:17]\1=[CH:18][CH:19]=[CH:20][CH:21]=2

参加物

6

実験手順

To a stirred slurry of potassium t-butoxide (4.7 g, 42.0 mmol) in 30 mL tetrahydrofuran at 0° C. is added ethyl isocyanoacetate (4.53 g, 40.0 mmol). This is stirred for 30 mins whereupon a solution of β-tetralone (5.88 g, 40.0 mmol) in tetrahydrofuran (20 mL) is added dropwise. The reaction mixture is allowed to warm to room temperature and stirred for 3 hours. The reaction mixture is then recooled in an ice bath and to this is added acetic acid (2.5 g, 41.6 mmol), allowed to warm to room temperature and stirred for an additional 30 mins. The solvent is removed in-vacuo and the residue partitioned between water and ethyl acetate. The organic layer is washed with water and brine, dried over sodium sulfate, filtered, evaporated and crystallized from cyclohexane to give 4.67 g of a white solid (contains some E-isomer), MS: m/z 260.2 (M+1).

後処理

  1. additionis added dropwise
  2. customThe reaction mixture is then recooled in an ice bath
  3. temperatureto warm to room temperature
  4. stirringstirred for an additional 30 mins
  5. customThe solvent is removed in-vacuo
  6. customthe residue partitioned between water and ethyl acetate
  7. washThe organic layer is washed with water and brine
  8. dry with materialdried over sodium sulfate
  9. filtrationfiltered
  10. customevaporated
  11. customcrystallized from cyclohexane

出典と根拠

ORDレコード
ord-a8160e7125b049a2b8a174406f9a3c0f
出典データセット
uspto-grants-2008_06
特許番号
US07390910B2

関連ノート

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