Ethanol → HCID 12287603, 화합물

HRID 865941노트

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HRID 865941 반응식
Cl.N=[C:3]([O:7][CH2:8][CH3:9])[CH:4]([CH3:6])[CH3:5].[CH2:10]([OH:12])[CH3:11].[CH3:13][CH2:14][O:15]CC>>[CH2:8]([O:7][C:3]([O:15][CH2:14][CH3:13])([O:12][CH2:10][CH3:11])[CH:4]([CH3:6])[CH3:5])[CH3:9]

참가 물질

4

실험 절차

To a suspension of 1-imino-1-ethoxyisobutane hydrochloride (610.0 g) in ether (12.5 L) was added ethanol (1940.0 g, 10 mol). The mixture was stirred at 35°-37° C. under N2 for 72 hours. The reaction mixture was filtered, the filtrate was washed with a 10% sodium carbonate solution, followed by a saturated sodium carbonate solution and the organic layer was dried over K2CO3. The organic layer was concentrated in vacuo and the residue was dissolved in ether, filtered and the filtrate was washed successively with a 10% NaOH solution and water. The organic layer was dried over K2CO3, the solvent was removed in vacuo and the residue was diluted with hexane, cooled in an ice-bath and filtered. The filtrate was concentrated in vacuo and the residue was distilled at 70°-72° C. (27 mmHg) to afford 320 g (42%) of 1,1,1-triethoxyisobutane.

후처리

  1. filtrationThe reaction mixture was filtered
  2. washthe filtrate was washed with a 10% sodium carbonate solution
  3. dry with materialthe organic layer was dried over K2CO3
  4. concentrationThe organic layer was concentrated in vacuo
  5. dissolutionthe residue was dissolved in ether
  6. filtrationfiltered
  7. washthe filtrate was washed successively with a 10% NaOH solution and water
  8. dry with materialThe organic layer was dried over K2CO3
  9. customthe solvent was removed in vacuo
  10. additionthe residue was diluted with hexane
  11. temperaturecooled in an ice-bath
  12. filtrationfiltered
  13. concentrationThe filtrate was concentrated in vacuo
  14. distillationthe residue was distilled at 70°-72° C. (27 mmHg)

출처 및 근거

ORD 기록
ord-59bf24b2c84549a58747eec171d24cf9
출처 데이터셋
uspto-grants-1996_10
특허 번호
US05569655

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