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Methyl iodide → Methyl 2-(2,4-dichlorophenyl)propanoate

HRID 745273
ノート
印刷プレビュー

反応式

HRID 745273 の反応式
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH2:9][C:10]([O:12][CH3:13])=[O:11].[H-].[Na+].I[CH3:17]>CN(C)C=O>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[CH:9]([CH3:17])[C:10]([O:12][CH3:13])=[O:11]
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 6328Methyl iodideHCID 24758Sodium hydrideHCID 2734106Methyl 2,4-dichlorobenzeneacetate

生成物 1

HCID 23315465Methyl 2-(2,4-dichlorophenyl)propanoate収率 80%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a stirred mixture of 22 parts of methyl 2,4-dichlorobenzeneacetate and 135 parts of N,N-dimethylformamide are added 3.1 parts of sodium hydride dispersion 78% while nitrogen gas is introduced. The whole is stirred till foaming has ceased and cooled in an ice-bath. Then there are added dropwise 16 parts of iodomethane. Upon completion, stirring is continued for 3 hours at room temperature. The reaction mixture is poured onto water and the product is extracted with 2,2'-oxybispropane. The extract is washed with water, dried, filtered and evaporated, yielding 20 parts (80%) of methyl 2,4-dichloro-α-methylbenzeneacetate as a residue.

後処理

  1. additionis introduced
  2. temperaturecooled in an ice-bath
  3. stirringUpon completion, stirring
  4. additionThe reaction mixture is poured onto water
  5. extractionthe product is extracted with 2,2'-oxybispropane
  6. washThe extract is washed with water
  7. customdried
  8. filtrationfiltered
  9. customevaporated

出典と根拠

ORDレコード
ord-a873e3eb455047f9ae7d6977df926573
出典データセット
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04598085

反応ノート

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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