反応 #2045065

ord-df721f204b904b80b0134168452f33d3

反応方程式

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
収率 87.6%

溶媒

反応条件

温度
110°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他Upon completion of the reaction
  2. 2
    洗浄the 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
    抽出extracted three times with AcOEt (50 ml×3)
  5. 5
    濃縮The combined AcOEt extracts were concentrated in vacuo
  6. 6
    その他purified via flash column chromatography with (0-40% gradient)

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08409649B2uspto-grants-2013_04