반응 #2045065

ord-df721f204b904b80b0134168452f33d3

반응 방정식

CCOC(=O)CCCC1CCC(C)C1(C)C
Ethyl 4-(2,2,3-trimethylcyclopentyl)butanoate
C1CCOC1
THF
CC1CCC(CCCC(=O)O)C1(C)C
4-(2,2,3-trimethylcyclopentyl)butanoic acid
수율 87.6%

용매

반응 조건

온도
110°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Upon completion of the reaction
  2. 2
    세척the aqueous layer washed twice with MTBE (50 ml×2)
  3. 3
    workup.ADDITIONThe aqueous layer was treated with aqueous 1.0 N HCl until it
  4. 4
    추출extracted three times with AcOEt (50 ml×3)
  5. 5
    농축The combined AcOEt extracts were concentrated in vacuo
  6. 6
    기타purified via flash column chromatography with (0-40% gradient)

실험 절차

Ethyl 4-(2,2,3-trimethylcyclopentyl)butanoate (5 g, 22 mmol) was added to THF (25 ml) into a round bottom flask. Aqueous 1 N NaOH (25 ml) was then added to the flask and the reaction mixture was refluxed at 110° C. for 8 h. Upon completion of the reaction, the reaction mixture was diluted with 1 N NaOH (25 ml) and the aqueous layer washed twice with MTBE (50 ml×2). The aqueous layer was treated with aqueous 1.0 N HCl until it reached a pH of about 3 (for example from 2 to 4), then extracted three times with AcOEt (50 ml×3). The combined AcOEt extracts were concentrated in vacuo and purified via flash column chromatography with (0-40% gradient) to give 4-(2,2,3-trimethylcyclopentyl)butanoic acid as a colorless oil (3.82 g, 87%). The NMR data is indicated below.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08409649B2uspto-grants-2013_04