Trifluoroacetic acid → 2-(trans-Dec4-en-1-ylamino)acetaldehyde dimethyl acetal

HRID 1062707ノート

反応式

HRID 1062707 の反応式
[CH:1](=O)[CH2:2][CH2:3]/[CH:4]=[CH:5]/[CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[CH3:12][O:13][CH:14]([O:17][CH3:18])[CH2:15][NH2:16].[BH3-]C#N.[Na+].C(O)(C(F)(F)F)=O>CO>[CH3:12][O:13][CH:14]([O:17][CH3:18])[CH2:15][NH:16][CH2:1][CH2:2][CH2:3]/[CH:4]=[CH:5]/[CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]

参加物

6

実験手順

trans-4-Decenal (7.2 g, 46.6 mmol) was mixed with 40 mL (0.37 moL) of aminoacetaldehyde dimethylacetal in 400 mL of methanol and stirred at room temperature for 30 minutes. NaCNBH3 (2.9 g, 46.6 mmol) was added, the reaction was cooled in an ice bath, and 27 mL (0.35 moL) of TFA was added dropwise over 5 minutes. The ice bath was then removed and the reaction was stirred for 70 minutes at room temperature, concentrated to a third of its volume, and partitioned between ethyl acetate (250 mL) and 1N NaOH (200 mL). The organic layer was washed with water (3×75 mL), dried over MgSO4 , filtered and concentrated under reduced pressure to yield 11.1 g (45.6 mmol) of 2-(trans-dec-4-en-1-ylamino)acetaldehyde dimethyl acetal as a yellow oil that was used directly in the next step.

後処理

  1. temperaturethe reaction was cooled in an ice bath
  2. customThe ice bath was then removed
  3. stirringthe reaction was stirred for 70 minutes at room temperature
  4. concentrationconcentrated to a third of its volume
  5. custompartitioned between ethyl acetate (250 mL) and 1N NaOH (200 mL)
  6. washThe organic layer was washed with water (3×75 mL)
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-021931ca32a44819a0a05fba5f4ac903
出典データセット
uspto-grants-2005_11
特許番号
US06962970B2

反応ノート

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