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Ethanol → Ethyl 5-hydroxynicotinate

HRID 509402
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HRID 509402 반응식
[OH:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([CH:10]=1)[C:7]([OH:9])=[O:8].OS(O)(=O)=O.CO.[CH3:18][CH2:19]O>C(Cl)(Cl)Cl>[OH:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([CH:10]=1)[C:7]([O:9][CH2:18][CH3:19])=[O:8]
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참가 물질

6

반응물 4

HCID 702Ethanol2회HCID 887MethanolHCID 1118Sulfuric AcidHCID 340375-Hydroxynicotinic acid

생성물 1

HCID 910016Ethyl 5-hydroxynicotinate

시약·촉매·용매 1

HCID 6212Chloroform용매

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온도
110 °C

실험 절차

To a stirred mixture of 5-hydroxynicotinic acid (25 g, 0.1797 mol, Combi Blocks) in EtOH (500 mL) was added a catalytic amount of conc. H2SO4. The resulting reaction mixture was stirred for 12 h at 110° C. After completion of the reaction (monitored by TLC, 10% MeOH in CHCl3), EtOH was removed under reduced pressure and the reaction mixture was quenched with sat'd NaHCO3 solution (50 mL) and extracted with EtOAc (50 mL×3). The combined organic layers were dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford the title compound as a solid. 1H NMR (400 MHz, CDCl3) δ: 11.00 (br.s., 1H), 8.74 (s, 1H), 8.42 (d, J=2.1 Hz, 1H), 7.90 (t, J=3.9 Hz, 1H), 4.43 (q, J=7.2 Hz, 2H), 1.43 (t, J=6.9 Hz, 3H). MS (ESI, positive ion) m/z: 168 (M+H).

후처리

  1. customThe resulting reaction mixture
  2. customwas removed under reduced pressure
  3. customthe reaction mixture was quenched with sat'd NaHCO3 solution (50 mL)
  4. extractionextracted with EtOAc (50 mL×3)
  5. dry with materialThe combined organic layers were dried over anhydrous sodium sulfate
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-d439821440304e7aa91fc3642e7d4892
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09096527B2

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