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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Phosphorus oxychloride → 3-Quinolinecarboxylic acid, 4-chloro-8-methoxy-, ethyl ester

HRID 66773
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HRID 66773 반응식
O[C:2]1[C:11]2[C:6](=[C:7]([O:12][CH3:13])[CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[C:14]([O:16][CH2:17][CH3:18])=[O:15].P(Cl)(Cl)([Cl:21])=O>C1(C)C=CC=CC=1>[Cl:21][C:2]1[C:11]2[C:6](=[C:7]([O:12][CH3:13])[CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[C:14]([O:16][CH2:17][CH3:18])=[O:15]
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참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 178469676HCID 178469676, 화합물

생성물 1

HCID 3045573-Quinolinecarboxylic acid, 4-chloro-8-methoxy-, ethyl ester수율 89%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A stirred mixture of ethyl 4-hydroxy-8-methoxyquinoline-3-carboxylate, 66.63 g (0.269 mole) and phosphorous oxychloride (350 ml) was warmed until all the solid had dissolved and then heated at reflux temperature for two hours. After cooling to below 100° C. the mixture was concentrated in a rotary evaporator. The residual oil was dissolved in 100 ml acetone and the solution poured onto an ice-water mixture (800 ml). The mixture was neutralized with 6 N sodium hydroxide solution and the solid product extracted successively with 450 ml, 250 ml and 100 ml portions of methylene chloride. The extracts were combined, washed with water, dried over anhydrous magnesium sulfate and concentrated to yield 68.16 g crude product. This crude product was dissolved in 500 ml hot toluene and filtered to remove a small quantity of insoluble material. The toluene solution was filtered through a bed of 250 g fluorisil followed by two liters of toluene and four liters of chloroform. The purified solution was concentrated to give 64.17 g of oil (89%) which crystallized to an off-white solid on cooling. The solid melted at 75°-77° C.

후처리

  1. temperaturewas warmed until all the solid
  2. dissolutionhad dissolved
  3. temperatureheated
  4. temperatureat reflux temperature for two hours
  5. temperatureAfter cooling to below 100° C. the mixture
  6. concentrationwas concentrated in a rotary evaporator
  7. dissolutionThe residual oil was dissolved in 100 ml acetone
  8. additionthe solution poured onto an ice-water mixture (800 ml)
  9. extractionthe solid product extracted successively with 450 ml, 250 ml and 100 ml portions of methylene chloride
  10. washwashed with water
  11. dry with materialdried over anhydrous magnesium sulfate
  12. concentrationconcentrated
  13. customto yield 68.16 g crude product
  14. filtrationfiltered
  15. customto remove a small quantity of insoluble material
  16. filtrationThe toluene solution was filtered through a bed of 250 g fluorisil
  17. concentrationThe purified solution was concentrated

출처 및 근거

ORD 기록
ord-8369daafd2564f97bd571732e2613eec
출처 데이터셋
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04343804

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