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Ammonia → 4-Bromo-2-methoxybenzamide

HRID 1804862
ノート
印刷プレビュー

反応式

HRID 1804862 の反応式
[Br:1][C:2]1[CH:11]=[CH:10][C:5]([C:6](OC)=[O:7])=[C:4]([O:12][CH3:13])[CH:3]=1.[OH-].[NH4+:15].[Cl-].[NH4+].N.Cl>>[Br:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([NH2:15])=[O:7])=[C:4]([O:12][CH3:13])[CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 5

HCID 222AmmoniaHCID 313Hydrochloric AcidHCID 14923Ammonium Hydroxide2 回HCID 25517Ammonium Chloride2 回HCID 15128242Methyl 4-bromo-2-methoxybenzoate

生成物 1

HCID 184570174-Bromo-2-methoxybenzamide収率 20.5%

実験手順

A mixture of methyl 4-bromo-2-methoxybenzoate (2.66 g, 10.85 mmol), 28% ammonium hydroxide (25 mL, 642 mmol) and ammonium chloride (2.0 g, 37.4 mmol) was stirred at RT for 20 min and then at 50° C. Once the material converted forms to an oil (ca. 20 min), the mixture was cooled to RT and more ammonium hydroxide (25 mL, 642 mmol) and ammonium chloride (2.0 g, 37.4 mmol) were added. Upon completion of addition, the reaction mixture was stirred at RT overnight. After this time, the mixture was heated to reflux in an open flask to drive off the excess ammonia and then cooled to RT. The mixture was neutralized with conc. HCl and then extracted with ethyl acetate. The extract was dried (Na2SO4) and then concentrated to give a residue. The residue was purified by flash chromatography (40 g silica gel cartridge; EtOAc/Hex) to give 4-bromo-2-methoxybenzamide (510 mg, 2.22 mmol, 20% yield) as a white solid.

後処理

  1. customat 50° C
  2. customto an oil (ca. 20 min)
  3. temperaturethe mixture was cooled to RT
  4. additionUpon completion of addition
  5. stirringthe reaction mixture was stirred at RT overnight
  6. temperatureAfter this time, the mixture was heated
  7. temperatureto reflux in an open flask
  8. temperaturecooled to RT
  9. extractionextracted with ethyl acetate
  10. dry with materialThe extract was dried (Na2SO4)
  11. concentrationconcentrated
  12. customto give a residue
  13. customThe residue was purified by flash chromatography (40 g silica gel cartridge; EtOAc/Hex)

出典と根拠

ORDレコード
ord-9939eef1965a4bbdbbf6ae898cc25319
出典データセット
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08354432B2

反応ノート

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