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4-Hydroxybenzoic Acid → 4-hydroxy-N-phenylbenzamide

HRID 2260947
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HRID 2260947 반응식
[OH:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=O)=[CH:4][CH:3]=1.[NH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.CCN=C=NCCCN(C)C>CN(C=O)C>[OH:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([NH:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[O:8])=[CH:9][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1354-Hydroxybenzoic AcidHCID 6115AnilineHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide

생성물 1

HCID 5647164-hydroxy-N-phenylbenzamide수율 29.2%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

4-Hydroxybenzoic acid (1.1 g, 7.96 mmoL) and aniline (742 mg, 7.23 mmol) were dissolved in 20 mL of dry DMF. To the above solution EDCI (1.53 g, 7.23 mmol) was added in one portion and the resulting mixture was stirred at rt overnight under nitrogen. The reaction mixture was then partitioned between EtOAc (200 mL) and water (200 mL). The organic layer was separated, washed consecutively with 1 N HCl, water, saturated sodium bicarbonate solution, water, and brine, and dried over MgSO4. Solvent was removed under reduced pressure and the crude product was purified by column chromatography using 10% EtOAc in hexane to give 450 mg (29% yield) of 4-Hydroxy-N-phenyl-benzamide. MS (ES) m/z: 214.08 (M+1).

후처리

  1. customThe reaction mixture was then partitioned between EtOAc (200 mL) and water (200 mL)
  2. customThe organic layer was separated
  3. washwashed consecutively with 1 N HCl, water, saturated sodium bicarbonate solution, water, and brine
  4. dry with materialdried over MgSO4
  5. customSolvent was removed under reduced pressure
  6. customthe crude product was purified by column chromatography

출처 및 근거

ORD 기록
ord-109404c252df4d07889f21c5b087c808
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07846915B2

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