HCID 54338605、化合物 → 1-[2,4-Bis(methoxymethoxy)phenyl]-3-(4-methoxymethoxyphenyl)-1-propanone

HRID 1030745

反応式

HRID 1030745 の反応式
[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:24]=[C:23]([O:25][CH2:26][O:27][CH3:28])[CH:22]=[CH:21][C:6]=1[C:7](=[O:20])[CH:8]=[CH:9][C:10]1[CH:15]=[CH:14][C:13]([O:16][CH2:17][O:18][CH3:19])=[CH:12][CH:11]=1>C(OCC)(=O)C.[Pd]>[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:24]=[C:23]([O:25][CH2:26][O:27][CH3:28])[CH:22]=[CH:21][C:6]=1[C:7](=[O:20])[CH2:8][CH2:9][C:10]1[CH:11]=[CH:12][C:13]([O:16][CH2:17][O:18][CH3:19])=[CH:14][CH:15]=1

参加物

4

反応物 1

HCID 54338605HCID 54338605、化合物

生成物 1

HCID 197448921-[2,4-Bis(methoxymethoxy)phenyl]-3-(4-methoxymethoxyphenyl)-1-propanone

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 8857Ethyl Acetate溶媒2 回

実験手順

Then, a suspension of 2.52 g of 5% palladium/carbon in 50 ml of ethyl acetate was hydrogenated for 2 hours, and a solution of 5.11 g of 2',4,4'-tris(methoxymethoxy)chalcone in 50 ml of ethyl acetate was added to the suspension and hydrogenation was carried out. After the reaction, the palladium/carbon was removed by filtration and the filtrate was concentrated under a reduced pressure to obtain 1-[2,4-bis(methoxymethoxy)phenyl]-3-(4-methoxymethoxyphenyl)-1-propanone.

後処理

  1. customAfter the reaction
  2. customthe palladium/carbon was removed by filtration
  3. concentrationthe filtrate was concentrated under a reduced pressure

出典と根拠

ORDレコード
ord-b83bb429686c41d5828f503d22c45b52
出典データセット
uspto-grants-1992_04
特許番号
US05106871

関連ノート

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