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

HRID 514242

反応式

HRID 514242 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

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 dilute sodium hydrogencarbonate solution was added. 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) gave 1.85 g (74% of theory) of ethyl 4-amino-2-chloro-5-iodobenzoate.

後処理

  1. filtrationThe reaction mixture was filtered through a frit
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. additiondilute sodium hydrogencarbonate solution was added
  4. customthe aqueous phase was removed
  5. dissolutionsodium thiosulphate was dissolved
  6. washThe organic phase was washed again with the aqueous phase
  7. extractionthe aqueous phase was extracted with ethyl acetate
  8. dry with materialThe combined organic phases were dried over sodium sulphate
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure
  11. 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-9cba2ea5e6944709ba4f889e37ea1d3c
出典データセット
uspto-grants-2015_08
特許番号
US09107411B2

関連ノート

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