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Ethanol → (Z)-Methyl 3-Methylhepta-2,6-dienoate

HRID 2251765
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HRID 2251765 반응식
C[Li].[C:3]([O:11][CH3:12])(=[O:10])[C:4]#[C:5][CH2:6][CH2:7][CH:8]=[CH2:9].[CH2:13](O)C>C1COCC1.CCOCC.[Cu]I>[CH3:13]/[C:5](/[CH2:6][CH2:7][CH:8]=[CH2:9])=[CH:4]/[C:3]([O:11][CH3:12])=[O:10]
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참가 물질

7

반응물 3

HCID 702EthanolHCID 59644062Methyl hept-6-en-2-ynoateHCID 178418348HCID 178418348, 화합물

생성물 1

HCID 59644092(Z)-Methyl 3-Methylhepta-2,6-dienoate수율 100%

시약·촉매·용매 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매HCID 3283
Diethyl Ether
용매
HCID 8028Tetrahydrofuran용매2회

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온도
-20 °C

실험 절차

A suspension of copper(I) iodide (12.38 g, 65 mmol) in 150 mL of dry THF under a nitrogen atmosphere was cooled to −20° C., and methyllithium (1.6 M in ether, 81.5 mL, 130 mmol) was added dropwise over 15 min. The solution was cooled to −78° C., and 4.49 g (32.5 mmol) of the compound from Example 19 in 15 mL of dry THF was added gradually, keeping the temperature below −70° C. After 1 h, 40 mL of ethanol was added cautiously, and the mixture was allowed to warm to room temperature. The mixture was diluted with ether, and washed with satd aq NH4Cl (200 mL), 5N NH3 (4×250 mL), water (200 mL), and brine (200 mL), dried, and the bulk of the solvent was evaporated to give the title compound (6.8 g, 100%) as an oil. The material had only minor solvent contamination and was adequate for use in the next reaction.

후처리

  1. temperatureThe solution was cooled to −78° C.
  2. customthe temperature below −70° C
  3. temperatureto warm to room temperature
  4. washwashed with satd aq NH4Cl (200 mL), 5N NH3 (4×250 mL), water (200 mL), and brine (200 mL)
  5. customdried
  6. customthe bulk of the solvent was evaporated

출처 및 근거

ORD 기록
ord-b9d332ec0a294673a4b222a949758680
출처 데이터셋
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07320974B2

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