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Hydrochloric Acid → Ethyl 3-(5-chloro-2-methoxyphenyl)-3-oxopropanoate

HRID 28554
ノート
印刷プレビュー

反応式

HRID 28554 の反応式
[Na+].[C:2]([O:8][CH2:9][CH3:10])(=[O:7])[CH2:3][C:4]([O-:6])=O.S([O-])([O-])(=O)=O.[Mg+2].C(N(CC)CC)C.[Cl:24][C:25]1[CH:26]=[CH:27][C:28]([O:38][CH3:39])=[C:29](C(N2C=CN=C2)=O)[CH:30]=1.[Cl-].[Mg+2].[Cl-].Cl>C(#N)C>[CH2:9]([O:8][C:2](=[O:7])[CH2:3][C:4]([C:27]1[CH:26]=[C:25]([Cl:24])[CH:30]=[CH:29][C:28]=1[O:38][CH3:39])=[O:6])[CH3:10]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 6

HCID 313Hydrochloric AcidHCID 8471TriethylamineHCID 24083Sulfuric acid magnesium salt (1:1)HCID 5360315Magnesium ChlorideHCID 23662308NatriummalonesterHCID 68987646(5-Chloro-2-methoxy-phenyl)-imidazol-1-yl-methanone

生成物 1

HCID 54012347
Ethyl 3-(5-chloro-2-methoxyphenyl)-3-oxopropanoate
収率 76%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

反応条件

温度
10 °C

実験手順

To a stirred mixture of ethyl malonate sodium salt (3.8 g, 24.7 mmol) and magnesium sulfate (3.2 g, 26.3 mmol) in acetonitrile (60 ml) was added triethylamine (4.7 ml, 33.5 mmol) under an argon atmosphere. After stirring for 2 hours, the solution containing (5-chloro-2-methoxy-phenyl)-imidazol-1-yl-methanone was added. After stirring at 80° C. for 2 hours, magnesium chloride (2.5 g, 26.3 mmol) was added and the mixture was stirred for 16 hours. After cooling to 10° C., concentrated hydrochloric acid (5 ml) was added and the mixture was stirred for 30 minutes. The layers were separated and the aqueous layer was extracted with ethyl acetate (3×60 ml). The combined organic layers were dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1:4 followed by 1:3) to provide 3-(5-chloro-2-methoxy-phenyl)-3-oxopropionic acid ethyl ester (2.3 g, 76% yield) as an oil. 1H NMR (CDCl3) δ 1.23 (t, 3H, J=8.7 Hz CH3), 3.89 (s, 3H, CH3), 3.94 (s, 2H, CH2), 4.17 (q, 2H, CH2), 6.91 (d, 1H, J=8.6 Hz, Ar), 7.45 (dd, 1H, J=8.8 Hz, J=2.6 Hz, Ar), 7.85 (d, 1H, J=2.6 Hz, Ar).

後処理

  1. additionwas added
  2. stirringAfter stirring at 80° C. for 2 hours
  3. stirringthe mixture was stirred for 16 hours
  4. stirringthe mixture was stirred for 30 minutes
  5. customThe layers were separated
  6. extractionthe aqueous layer was extracted with ethyl acetate (3×60 ml)
  7. dry with materialThe combined organic layers were dried over magnesium sulfate
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1:4 followed by 1:3)

出典と根拠

ORDレコード
ord-bdb4a6607416413d9cebb779de9ff903
出典データセット
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07419984B2

反応ノート

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