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Benzaldehyde → Methyl 2-(1-oxopropyl)-3-(4-fluorophenyl)-4-phenyl-4-oxobutanoate

HRID 2107087
ノート
印刷プレビュー

反応式

HRID 2107087 の反応式
[F:1][C:2]1[CH:17]=[CH:16][C:5]([CH:6]=[C:7]([C:12](=[O:15])[CH2:13][CH3:14])[C:8]([O:10][CH3:11])=[O:9])=[CH:4][CH:3]=1.[CH:18](=[O:25])[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.C(N(CC)CC)C.C(O)C>[I-].C[N+]1C(C)=C(CCO)SC=1.ClCCl>[O:15]=[C:12]([CH:7]([CH:6]([C:5]1[CH:4]=[CH:3][C:2]([F:1])=[CH:17][CH:16]=1)[C:18]([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)=[O:25])[C:8]([O:10][CH3:11])=[O:9])[CH2:13][CH3:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 240BenzaldehydeHCID 702EthanolHCID 8471TriethylamineHCID 53755005Methyl 2-(4-fluorobenzylidene)-3-oxopentanoate

生成物 1

HCID 23047461Methyl 2-(1-oxopropyl)-3-(4-fluorophenyl)-4-phenyl-4-oxobutanoate収率 28.5%

試薬・触媒・溶媒 2

HCID 9838770
3,4-Dimethyl-5-(2-hydroxyethyl)thiazolium iodide
触媒
HCID 6344Dichloromethane溶媒

実験手順

A mixture of methyl 2-(4-fluorobenzylidene)-3-oxopentanoate (52.0 g), benzaldehyde (25.4 g), triethylamine (22 g), 3,4-dimethyl-5-(2-hydroxyethyl)thiazolium iodide (6.3 g) and ethanol (100 ml) was heated at reflux under nitrogen for 16 hours. The cooled mixture was diluted with dichloromethane, and washed with dilute hydrochloric acid (2N), with dilute aqueous sodium bicarbonate solution, and with water, and dried over magnesium sulphate. The solution was concentrated in vacuo and the residue was dissolved in hot methanol. The resulting off-white solid was filtered off, to give methyl 2-(1-oxopropyl)-3-(4-fluorophenyl)-4-phenyl-4-oxobutanoate (21.5 g), m.p. 104°-109° C. [Elemental analysis: C,70.1;H,5.42;F,5.58%; calculated: C,70.15;H,5.60; F,5.55%; I.R. 1749, 1738, 1716, 1708, 1679, 1508, 761, 697cm-1 [N.M.R. (in CDCl3): 0.81 and 1.08 (3H, two triplets, J=7 Hz), 1.80-2.04 and 2.46-2.80 (2H, two sets of multiplets), 3.53 and 3.68 (3H, two singlets), 4.58 and 4.62 (1H, two doublets, J=10 Hz), 5.39 and 5.42 (1H, two doublets, J=10 Hz), 6.96 (2H, t, J=8 Hz), 7.20- 7.60 (5H, m), 7.90-8.00 (2H, m)].

後処理

  1. temperaturewas heated
  2. temperatureat reflux under nitrogen for 16 hours
  3. washwashed with dilute hydrochloric acid (2N), with dilute aqueous sodium bicarbonate solution
  4. dry with materialwith water, and dried over magnesium sulphate
  5. concentrationThe solution was concentrated in vacuo
  6. dissolutionthe residue was dissolved in hot methanol
  7. filtrationThe resulting off-white solid was filtered off

出典と根拠

ORDレコード
ord-64489adf48f149e6a120ce7a2bd1f8c2
出典データセット
uspto-grants-1990_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04933350

反応ノート

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