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Formic Acid → N-formyl-2-amino-3',5-di-t-butyl biphenyl

HRID 606686
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HRID 606686 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:11])([CH3:10])[CH3:9])=[CH:4][C:3]=1[C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([CH3:21])([CH3:20])[CH3:19])[CH:13]=1.[CH:22](O)=[O:23]>O>[CH:22]([NH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:9])([CH3:10])[CH3:11])=[CH:4][C:3]=1[C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([CH3:21])([CH3:20])[CH3:19])[CH:13]=1)=[O:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 284Formic AcidHCID 66813837HCID 66813837, 화합물

생성물 1

HCID 86614227N-formyl-2-amino-3',5-di-t-butyl biphenyl수율 82%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Added 2-amino-3′,5-di-t-butyl biphenyl (2.0 g, 7.11 mmol) to a solution of formic acid and heated to reflux for 16 hours. After cooling, water (25 mL) was added the product and the precipitate collected by vacuum filtration. The crude product was dissolved into ethyl acetate, washed with water. The organics were dried over magnesium sulfate and concentrated and purified by column chromatography using 10% ethyl acetate and hexanes as the eluants to give the pure N-formyl-2-amino-3′,5-di-t-butyl biphenyl (1.8 g, 82% yield) as determined by GCMS.

후처리

  1. temperatureheated
  2. temperatureto reflux for 16 hours
  3. temperatureAfter cooling
  4. filtrationthe precipitate collected by vacuum filtration
  5. dissolutionThe crude product was dissolved into ethyl acetate
  6. washwashed with water
  7. dry with materialThe organics were dried over magnesium sulfate
  8. concentrationconcentrated
  9. custompurified by column chromatography

출처 및 근거

ORD 기록
ord-320c4914865843878d96563b2e322d2e
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07915415B2

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