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methyl 5-(3-cyclopentoxy-4-methoxyphenyl)-2,4-E,E-pentadienoate → Methyl 5-(3-cyclopentoxy-4-methoxyphenyl)-n-pentanoate

HRID 327602
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반응식

HRID 327602 반응식
[CH:1]1([O:6][C:7]2[CH:8]=[C:9](/[CH:15]=[CH:16]/[CH:17]=[CH:18]/[C:19]([O:21][CH3:22])=[O:20])[CH:10]=[CH:11][C:12]=2[O:13][CH3:14])[CH2:5][CH2:4][CH2:3][CH2:2]1.[H][H]>[Pd].CO>[CH:1]1([O:6][C:7]2[CH:8]=[C:9]([CH2:15][CH2:16][CH2:17][CH2:18][C:19]([O:21][CH3:22])=[O:20])[CH:10]=[CH:11][C:12]=2[O:13][CH3:14])[CH2:2][CH2:3][CH2:4][CH2:5]1
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참가 물질

5

반응물 2

HCID 15052472methyl 5-(3-cyclopentoxy-4-methoxyphenyl)-2,4-E,E-pentadienoateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 15052476Methyl 5-(3-cyclopentoxy-4-methoxyphenyl)-n-pentanoate

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of 0.20 g (0.66 mmol) of methyl 5-(3-cyclopentoxy-4-methoxyphenyl)-2,4-E,E-pentadienoate 75 mL of methanol is added 0.05 g of 5% palladium on carbon black. The suspension is shaken under a 50 psi atmosphere of hydrogen for 52 minutes after which time the excess gas is dissociated and the solution is filtered over Celite 545. The mixture is concentrated to dryness followed by liquid chromatography of the crude product over 100 g of silica gel eluting with 7.5% ethyl acetate in hexane. The final product is dried in vacuo and is found to be as analytically pure as an oil.

후처리

  1. filtrationthe solution is filtered over Celite 545
  2. concentrationThe mixture is concentrated to dryness
  3. dry with materialThe final product is dried in vacuo

출처 및 근거

ORD 기록
ord-39c2c80f52ff45138b293983d532080e
출처 데이터셋
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05274002

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