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Propionic Acid → HCID 67330102、化合物

HRID 2408243
ノート
印刷プレビュー

反応式

HRID 2408243 の反応式
[C:1](OC)([O:5][CH3:6])([O:3]C)[CH3:2].[C:9]1([CH:15](O)[C:16]([CH3:18])=[CH2:17])[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.C(O)(=O)CC>CO>[CH3:17]/[C:16](=[CH:15]\[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)/[CH2:18][CH2:2][C:1]([O:5][CH3:6])=[O:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 1032Propionic AcidHCID 15050Trimethyl orthoacetateHCID 1382112-Methyl-1-phenyl-2-propen-1-ol

生成物 1

HCID 67330102HCID 67330102、化合物収率 21%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Trimethyl orthoacetate (186 g, 1.52 mol) and 1-phenyl-2-methyl-2-propen-1-ol (90% pure from Alfa Aesar, 25 g, 0.152 mol) were heated in the presence of propionic acid (0.2 ml) in an oil bath at 145° C. for 4 hours. The methanol formed during the reaction was distilled. The excess orthoacetate was then removed under vacuum and the residue was purified by column chromatography on silica gel (eluent: heptanes/ethyl acetate 25:1 to 8:1) followed by bulb-to-bulb distillation (67° C./0.001 mbar). 6.5 g (yield=21%) of the desired product were obtained.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. distillationwas distilled
  2. customThe excess orthoacetate was then removed under vacuum
  3. customthe residue was purified by column chromatography on silica gel (eluent: heptanes/ethyl acetate 25:1 to 8:1)
  4. distillationfollowed by bulb-to-bulb distillation (67° C./0.001 mbar)

出典と根拠

ORDレコード
ord-d30270d395fc49209f089ff6d6301b15
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08815792B2

反応ノート

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