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Methyl formate → Ethyl 4-tert-butyl-5-chloro-2-ethoxybenzoate

HRID 2425588
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HRID 2425588 반응식
[C:1]([C:5]1[C:10]([Cl:11])=[CH:9][C:8](I)=[C:7]([O:13][CH2:14][CH3:15])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[CH3:16][O-].[Na+].[CH3:19][O:20][CH:21]=[O:22]>O1CCOCC1>[C:1]([C:5]1[C:10]([Cl:11])=[CH:9][C:8]([C:21]([O:20][CH2:19][CH3:16])=[O:22])=[C:7]([O:13][CH2:14][CH3:15])[CH:6]=1)([CH3:4])([CH3:3])[CH3:2]
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참가 물질

5

반응물 3

HCID 7865Methyl formateHCID 10942334Sodium MethoxideHCID 672462864-Tert-butyl-5-chloro-2-ethoxy-1-iodobenzene

생성물 1

HCID 67245813Ethyl 4-tert-butyl-5-chloro-2-ethoxybenzoate수율 80%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매2회

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온도
60 °C

실험 절차

To a degassed solution of 4-tert-butyl-5-chloro-2-ethoxy-1-iodobenzene (2.2 g, 6.4 mmol), sodium methoxide (0.52 g, 9.6 mmol) and dichlorobistriphenylphosphinepalladium (0.25 g, 0.4 mmol) in dioxane (20 mL) was added methylformate (1.2 mL, 19.4 mmol). The resulting mixture was heated in an oil bath (60° C.) for 18 h and then allowed to cool. The solution was diluted with dioxane and filtered through a plug of Celite and concentrated. Purification of the crude residue by flash chromatography over silica gel using 5-20% ethyl acetate in hexanes gave ethyl 4-tert-butyl-5-chloro-2-ethoxybenzoate (1.39 g, 80%) as a clear oil.

후처리

  1. temperatureto cool
  2. filtrationfiltered through a plug of Celite
  3. concentrationconcentrated
  4. customPurification of the crude residue by flash chromatography over silica gel using 5-20% ethyl acetate in hexanes

출처 및 근거

ORD 기록
ord-7f24652838d440f38232ada8f530c928
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07964724B2

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