Potassium Hydroxide → 5-(3-Methoxyphenyl)-1,2,3,6-tetrahydropyridine

HRID 851136노트

반응식

HRID 851136 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:9]2[CH2:10][N:11](C(OCC)=O)[CH2:12][CH2:13][CH:14]=2)[CH:6]=[CH:7][CH:8]=1.[OH-].[K+]>C(O)CCC.O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:9]2[CH2:10][NH:11][CH2:12][CH2:13][CH:14]=2)[CH:6]=[CH:7][CH:8]=1

참가 물질

5

반응물 2

HCID 14797Potassium HydroxideHCID 20502638Ethyl 3-(3-methoxyphenyl)-1,2,5,6-tetrahydro-1-pyridine-carboxylate

생성물 1

HCID 130667485-(3-Methoxyphenyl)-1,2,3,6-tetrahydropyridine수율 100.4%

시약·촉매·용매 2

HCID 2631-Butanol용매HCID 962Water용매

실험 절차

A solution of 11 g of the product of Step C in 110 ml of n-butanol and 11 g of potassium hydroxide was heated for 6 hours at 120° C. and the mixture was cooled and diluted with water. The mixture was extracted with ethyl acetate and the organic phase was washed with aqueous saturated sodium chloride solution, dried and evaporated to dryness under reduced pressure. The residue was chromatographed over silica gel and was eluted with a 6-3-1 chloroform-acetone-triethylamine mixture. The distilled fraction residue was taken up in methylene chloride and the solution was filtered and evaporated to dryness under reduced pressure to obtain 8 g of 3-(3-methoxyphenyl)-1,2,5,6-tetrahydropyridine.

후처리

  1. temperaturethe mixture was cooled
  2. extractionThe mixture was extracted with ethyl acetate
  3. washthe organic phase was washed with aqueous saturated sodium chloride solution
  4. customdried
  5. customevaporated to dryness under reduced pressure
  6. customThe residue was chromatographed over silica gel
  7. washwas eluted with a 6-3-1 chloroform-acetone-triethylamine mixture
  8. filtrationthe solution was filtered
  9. customevaporated to dryness under reduced pressure

출처 및 근거

ORD 기록
ord-eb70860f017f41c9ad9e1dfc9a88fb6e
출처 데이터셋
uspto-grants-1983_05
특허 번호
US04382942

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