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Acetonitrile → Ethyl 3-chloro-4-iodo-5-methoxybenzoate

HRID 1971777
ノート
印刷プレビュー

反応式

HRID 1971777 の反応式
N[C:2]1[C:12]([O:13][CH3:14])=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][C:3]=1[Cl:15].C(#N)C.[I:19]CI.N(OCCC(C)C)=O>CCCCCCC.C(OCC)(=O)C>[Cl:15][C:3]1[CH:4]=[C:5]([CH:11]=[C:12]([O:13][CH3:14])[C:2]=1[I:19])[C:6]([O:8][CH2:9][CH3:10])=[O:7]
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

6

反応物 4

HCID 6342AcetonitrileHCID 6346DiiodomethaneHCID 8053Isoamyl NitriteHCID 57912463Ethyl 4-amino-3-chloro-5-methoxybenzoate

生成物 1

HCID 57912451Ethyl 3-chloro-4-iodo-5-methoxybenzoate収率 66.6%

試薬・触媒・溶媒 1

HCID 21899848Ethylacetate heptane
溶媒

反応条件

温度
70 °C

実験手順

To ethyl 4-amino-3-chloro-5-methoxybenzoate (15.8 g, 68.8 mmol) were added acetonitrile (40 mL) and diiodomethane (22.2 mL, 275 mmol) in that order, and then the mixture was stirred at 70° C. and isoamyl nitrite (13.9 mL, 103 mmol) was added dropwise over a period of 10 minutes. The mixture was then stirred at 70° C. for 40 minutes. After returning the mixture to room temperature, the solvent in the mixture was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (mixture of n-heptane and ethyl acetate: n-heptane/ethyl acetate=8/1 then 5/1) to obtain the title compound (15.6 g, 45.8 mmol).

後処理

  1. stirringThe mixture was then stirred at 70° C. for 40 minutes
  2. customto room temperature
  3. distillationthe solvent in the mixture was distilled off under reduced pressure
  4. customthe residue was purified by silica gel column chromatography (
  5. additionmixture of n-heptane and ethyl acetate

出典と根拠

ORDレコード
ord-cfae15e6fc0f46c9a0f38139eac18d33
出典データセット
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08431603B2

反応ノート

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