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

HRID 28449
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HRID 28449 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]
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참가 물질

8

반응물 5

HCID 7912DiisopropylamineHCID 11039Methyl isobutyrateHCID 816462(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 5275811-Iodo-4-methylpentaneHCID 178418339Butyllithium

생성물 1

HCID 216784792,2,6-Trimethyl-heptanoic acid methyl ester수율 99.4%

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매2회HCID 8058Hexane용매

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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-35517808fb2c4f85bbc4e95e78c9c6e4
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07419981B2

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