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Phosphorus oxychloride → Methyl 4-(3-chloro-1,2,4-triazin-6-yl)benzoate

HRID 500217
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HRID 500217 반응식
O=[C:2]1[N:7]=[CH:6][C:5]([C:8]2[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[CH:10][CH:9]=2)=[N:4][NH:3]1.P(Cl)(Cl)([Cl:20])=O>C(Cl)(Cl)Cl>[Cl:20][C:2]1[N:3]=[N:4][C:5]([C:8]2[CH:17]=[CH:16][C:11]([C:12]([O:14][CH3:15])=[O:13])=[CH:10][CH:9]=2)=[CH:6][N:7]=1
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참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 59216301Methyl 4-(3-oxo-2,3-dihydro-1,2,4-triazin-6-yl)benzoate

생성물 1

HCID 59216349Methyl 4-(3-chloro-1,2,4-triazin-6-yl)benzoate수율 17.3%

시약·촉매·용매 1

HCID 6212Chloroform용매

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온도
100 °C

실험 절차

A mixture of methyl 4-(3-oxo-2,3-dihydro-1,2,4-triazin-6-yl)benzoate (13.4 g, 0.0580 mol), phosphoryl chloride (30 mL, 0.3 mol) in chloroform (50 mL) was refluxed (oil-bath temperature about 100° C.) for 2 h. After cooling to RT, the mixture was concentrated to remove excess phosphoryl chloride. The residue was dissolved in methylene chloride and poured into ice-water, and carefully neutralized with K2CO3. The organic layer was separated and the aqueous solution was extracted with methylene chloride. The combined organic phases were dried over Na2SO4, concentrated, and further purified by chromatography to afford the desired product (2.5 g, 17%). LCMS: (M+H)=249.9. 1H NMR (300 MHz, CDCl3): in ppm, 3.98 (s, 3H), 8.18 (d, 2H), 8.24 (d, 2H), 8.96 (s, 1H).

후처리

  1. temperatureAfter cooling to RT
  2. concentrationthe mixture was concentrated
  3. customto remove excess phosphoryl chloride
  4. dissolutionThe residue was dissolved in methylene chloride
  5. additionpoured into ice-water
  6. customThe organic layer was separated
  7. extractionthe aqueous solution was extracted with methylene chloride
  8. dry with materialThe combined organic phases were dried over Na2SO4
  9. concentrationconcentrated
  10. customfurther purified by chromatography

출처 및 근거

ORD 기록
ord-1f813a8653c54376ae6f11b4566f88e3
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07767675B2

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