Diisopropylamine → 2,2,6-Trimethyl-heptanoic acid methyl ester

HRID 1829847

반응식

HRID 1829847 반응식
C(NC(C)C)(C)C.[Li]CCCC.[C:13]([O:18][CH3:19])(=[O:17])[CH:14]([CH3:16])[CH3:15].I[CH2:21][CH2:22][CH2:23][CH:24]([CH3:26])[CH3:25].CN1C(=O)N(C)CCC1>C1COCC1.CCCCCC>[CH3:19][O:18][C:13](=[O:17])[C:14]([CH3:16])([CH3:15])[CH2:21][CH2:22][CH2:23][CH:24]([CH3:26])[CH3:25]

참가 물질

8

반응 조건

온도
-78 °C

실험 절차

To diisopropyl amine (1.54 mL, 11.03 mmol) in THF (22 mL) at −78° C. was added nBuLi (6.89 mL of a 1.6 M solution in hexane). The solution was stirred for 30 min at −78° C., followed by the addition of methyl isobutyrate (0.97 mL, 8.48 mmol). The mixture was stirred at −78° C. for 2 h, and then 1-iodo-4-methyl pentane (1.8 g, 8.48 mmol) and DMPU (0.55 mL, 4.24 mmol) in THF (6 mL) was added. The reaction was stirred at −78° C. and allowed to slowly reach ambient temperature over 16 h. The reaction was quenched by the addition of ammonium chloride (saturated aqueous solution), and the mixture was extracted with EtOAc (2×10 mL). The organics were combined, washed with water, dried (MgSO4), filtered and concentrated. Silica gel chromatography (99/1 hexane/EtOAc) provided 1.57 g of 2,2,6-Trimethyl-heptanoic acid methyl ester.

후처리

  1. stirringThe mixture was stirred at −78° C. for 2 h
  2. stirringThe reaction was stirred at −78° C.
  3. waitallowed to slowly reach ambient temperature over 16 h
  4. customThe reaction was quenched by the addition of ammonium chloride (saturated aqueous solution)
  5. extractionthe mixture was extracted with EtOAc (2×10 mL)
  6. washwashed with water
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-e110ae215e8a4d98a7584b463aa339e1
출처 데이터셋
uspto-grants-2006_06
특허 번호
US07064147B2

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