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Acetic Anhydride → N-[(2-Hydroxyphenyl)methyl]acetamide

HRID 1782028
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HRID 1782028 반응식
C[O:2][C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[CH2:5][NH2:6].[C:11](OC(=O)C)(=[O:13])[CH3:12]>CO>[OH:2][C:3]1[CH:10]=[CH:9][CH:8]=[CH:7][C:4]=1[CH2:5][NH:6][C:11](=[O:13])[CH3:12]
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참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 812922-Methoxybenzylamine

생성물 1

HCID 12714526N-[(2-Hydroxyphenyl)methyl]acetamide수율 40.4%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
0 °C

실험 절차

2-Methoxybenzylamine (822 mg, 6.0 mmol) in methanol (10 mL) was treated with acetic anhydride (613 mg, 6.0 mmol) at room temperature for 2 h. The volatiles were removed in vacuo. The residue was dissolved in CH2Cl2, cooled to 0° C., 1M solution of BBr3 in CH2Cl2 (12 mL, 12.0 mml) was added slowly. After addition was completed the reaction mixture was stirred at room temperature overnight, cooled to 0° C., methanol (3 mL) was added and after 10 min volatiles were removed in vacuo. The residue was dissolved in ethyl acetate, washed successively with aqueous NaHCO3 and H2O. The organic layer was dried over Na2SO4 filtered and concentrated. The residue was purified by silica gel flash chromatography (0-50% ethyl acetate in petroleum spirit) to give the subtitled compound (400 mg).

후처리

  1. customThe volatiles were removed in vacuo
  2. dissolutionThe residue was dissolved in CH2Cl2
  3. addition1M solution of BBr3 in CH2Cl2 (12 mL, 12.0 mml) was added slowly
  4. additionAfter addition
  5. temperaturecooled to 0° C.
  6. additionmethanol (3 mL) was added and after 10 min volatiles
  7. customwere removed in vacuo
  8. dissolutionThe residue was dissolved in ethyl acetate
  9. washwashed successively with aqueous NaHCO3 and H2O
  10. dry with materialThe organic layer was dried over Na2SO4
  11. filtrationfiltered
  12. concentrationconcentrated
  13. customThe residue was purified by silica gel flash chromatography (0-50% ethyl acetate in petroleum spirit)

출처 및 근거

ORD 기록
ord-e72c213d05474d4890d4901341c88629
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07498338B2

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