HCID 15052473, compound → HCID 15052477, compound

HRID 327603Notes

Reaction equation

HRID 327603 reaction equation
[CH:1]1([O:6][C:7]2[CH:8]=[C:9](/[CH:15]=[CH:16]/[CH:17]=[CH:18]/[CH:19]=[CH:20]/[C:21]([O:23][CH3:24])=[O:22])[CH:10]=[CH:11][C:12]=2[O:13][CH3:14])[CH2:5][CH2:4][CH2:3][CH2:2]1.[H][H]>CO.[Pd]>[CH:1]1([O:6][C:7]2[CH:8]=[C:9]([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][C:21]([O:23][CH3:24])=[O:22])[CH:10]=[CH:11][C:12]=2[O:13][CH3:14])[CH2:2][CH2:3][CH2:4][CH2:5]1

Participants

5

Procedure

To a solution of 0.52 g (1.58 mmol) of methyl 7-(3-cyclopentoxy-4-methoxyphenyl)-2,4,6-E,E,E-heptatrienoate in 100 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 16 hours 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.

Workup

  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

Sources & evidence

ORD record
ord-3e06b1decca344bcbf3b614b35c26ae5
Source dataset
uspto-grants-1993_12
Patent number
US05274002

Reaction notes

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