alpha-Naphthaleneacetic acid, ethyl ester → Diethyl 2-(1-naphthyl)malonate

HRID 1613332

반응식

HRID 1613332 반응식
[C:1]1([CH2:11][C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[C:17](=O)([O-:21])[O:18][CH2:19][CH3:20].[O-]CC.[Na+].[Na]>C(O)C>[C:1]1([CH:11]([C:17]([O:18][CH2:19][CH3:20])=[O:21])[C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1

참가 물질

6

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온도
105 °C

실험 절차

A mixture of 103.9 g (485 mmol) of ethyl naphthalene-1-acetate and 430 ml of ethyl carbonate is stirred at 105° C., and a solution of sodium ethoxide (11 g (478 mmol) of sodium in 255 ml of absolute ethanol) is then added in such a way that the ethanol distils in the course of the introduction. The mixture is heated for a further 15 min. to distil the maximum amount of ethanol, the flask is rapidly cooled and the mixture is poured onto 300 g of crushed ice and 20 ml of concentrated hydrochloric acid. It is extracted with diethyl ether, the organic phase is dried over magnesium sulphate and filtered, and the solvent is evaporated under reduced pressure. An oil is obtained which crystallises in pentane in the cold. The crystals are separated by filtration, treated with vegetable charcoal in diethyl ether and filtered, the filtrate is evaporated and the residue is recrystallised in a 25:75 mixture of diethyl ether/pentane. 97 g (339 mmol) of crystals are obtained.

후처리

  1. customdistils in the course of the introduction
  2. temperatureThe mixture is heated for a further 15 min.
  3. customto distil the maximum amount of ethanol
  4. temperaturethe flask is rapidly cooled
  5. additionthe mixture is poured onto 300 g of crushed ice and 20 ml of concentrated hydrochloric acid
  6. extractionIt is extracted with diethyl ether
  7. dry with materialthe organic phase is dried over magnesium sulphate
  8. filtrationfiltered
  9. customthe solvent is evaporated under reduced pressure
  10. customAn oil is obtained which
  11. customcrystallises in pentane in the cold
  12. customThe crystals are separated by filtration
  13. additiontreated with vegetable charcoal in diethyl ether
  14. filtrationfiltered
  15. customthe filtrate is evaporated
  16. customthe residue is recrystallised in a 25:75 mixture of diethyl ether/pentane

출처 및 근거

ORD 기록
ord-46828f382bbf4f77a27019604f3708f7
출처 데이터셋
uspto-grants-1993_03
특허 번호
US05192797

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