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Methyl iodide → Ethyl 2-(2-chloropyridin-4-yl)propanoate

HRID 2069057
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HRID 2069057 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH:5]=[CH:4][N:3]=1.[CH3:14][Si]([N-][Si](C)(C)C)(C)C.[K+].CI.[NH4+].[Cl-]>C1COCC1.CCOCC>[Cl:1][C:2]1[CH:7]=[C:6]([CH:8]([CH3:14])[C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH:5]=[CH:4][N:3]=1
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참가 물질

7

반응물 4

HCID 6328Methyl iodideHCID 25517Ammonium ChlorideHCID 3251421Potassium bis(trimethylsilyl)amideHCID 57709236Ethyl 2-(2-chloropyridin-4-yl)acetate

생성물 1

HCID 58532560Ethyl 2-(2-chloropyridin-4-yl)propanoate수율 58.7%

시약·촉매·용매 2

HCID 3283
Diethyl Ether
용매
HCID 8028Tetrahydrofuran용매

실험 절차

To a stirred solution of ethyl 2-(2-chloropyridin-4-yl)acetate (44) (2.5 g, 12.52 mmol) in THF (25 mL), under nitrogen at −78° C. was added a solution of KHMDS (0.5M in toluene, 26.3 mL, 13.2 mmol). The mixture was warmed to RT for 10 min, then re-cooled to −78° C. and methyl iodide (0.820 mL, 13.15 mmol) added in a single portion and the mixture allowed to warm to RT. Saturated aqueous NH4Cl solution was added and the mixture was diluted with ether. The organic layer was washed with water and brine and then dried (MgSO4) and evaporated in vacuo. The residue was purified by flash column chromatography (SiO2, 100 g, 5-10% EtOAc in isohexane, gradient elution) to afford the title compound (51) (1.57 g, 56%): m/z 214 (M+H)+ (ES+).

후처리

  1. temperaturere-cooled to −78° C.
  2. temperatureto warm to RT
  3. washThe organic layer was washed with water and brine
  4. dry with materialdried (MgSO4)
  5. customevaporated in vacuo
  6. customThe residue was purified by flash column chromatography (SiO2, 100 g, 5-10% EtOAc in isohexane, gradient elution)

출처 및 근거

ORD 기록
ord-317a700bc2cb439fab0e4f357e09ab54
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08299073B2

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