Iodine → Ethyl 4-amino-2-chloro-5-iodobenzoate

HRID 339114

反応式

HRID 339114 の反応式
[I:1]I.[NH2:3][C:4]1[CH:14]=[CH:13][C:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[C:6]([Cl:15])[CH:5]=1>C(O)C.S([O-])([O-])(=O)=O.[Ag+].[Ag+]>[NH2:3][C:4]1[C:14]([I:1])=[CH:13][C:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[C:6]([Cl:15])[CH:5]=1

参加物

5

反応物 2

HCID 807IodineHCID 13287887Ethyl 4-amino-2-chlorobenzoate

生成物 1

HCID 58247958Ethyl 4-amino-2-chloro-5-iodobenzoate

試薬・触媒・溶媒 2

HCID 159865Silver sulfate触媒HCID 702Ethanol溶媒

実験手順

An iodine solution in ethanol was admixed with silver(I) sulphate and ethyl 4-amino-2-chlorobenzoate and then stirred at room temperature for 45 min. The reaction mixture was filtered through a frit and the filtrate was concentrated under reduced pressure. The residue was slurried in EtOAc and admixed with dilute sodium hydrogencarbonate solution. Once everything had gone into solution, the aqueous phase was removed and sodium thiosulphate was dissolved therein. The organic phase was washed again with the aqueous phase, and the aqueous phase was extracted with ethyl acetate. The combined organic phases were dried over sodium sulphate, filtered and concentrated under reduced pressure. Column chromatography purification on silica gel with cyclohexane/ethyl acetate as the eluent (gradient from 10% ethyl acetate to 33% ethyl acetate).

後処理

  1. filtrationThe reaction mixture was filtered through a frit
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. customthe aqueous phase was removed
  4. dissolutionsodium thiosulphate was dissolved
  5. washThe organic phase was washed again with the aqueous phase
  6. extractionthe aqueous phase was extracted with ethyl acetate
  7. dry with materialThe combined organic phases were dried over sodium sulphate
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customColumn chromatography purification on silica gel with cyclohexane/ethyl acetate as the eluent (gradient from 10% ethyl acetate to 33% ethyl acetate)

出典と根拠

ORDレコード
ord-843454d3a09446a7bfa51292b6a62085
出典データセット
uspto-grants-2014_11
特許番号
US08889878B2

関連ノート

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