反応 #2186198

ord-ea436ee646474ad3b1fcd5f35788c6be

反応方程式

Oc1ccc2c(c1)NCCC2
1,2,3,4-Tetrahydro-quinolin-7-ol
FCCBr
1-bromo-2-fluoroethane
CCN(C(C)C)C(C)C
diisopropylethylamine
Oc1ccc2c(c1)N(CCF)CCC2
desired product
収率 44.0%
Oc1ccc2c(c1)N(CCF)CCC2
1-(2-Fluoro-ethyl)-1,2,3,4-tetrahydro-quinolin-7-ol
収率 44.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    抽出The reaction mixture is extracted with 0.1 N aqu
  2. 2
    洗浄The combined organic extracts are washed with brine
  3. 3
    乾燥dried over sodium acetate
  4. 4
    その他evaporated
  5. 5
    その他chromatographed (silica gel, ethyl acetate/petroleum ether 1:2 to 1:1)

実験手順

500 mg (3.35 mmol) 1,2,3,4-Tetrahydro-quinolin-7-ol are dissolved in 8 mL DMF and stirred at 60° C. overnight with 0.325 mL (1.3 eq) 1-bromo-2-fluoroethane, in the presence of 0.63 mL (1.1 eq) diisopropylethylamine. The reaction mixture is extracted with 0.1 N aqu. HCl and ethyl acetate. The combined organic extracts are washed with brine, dried over sodium acetate and evaporated. The residue is column chromatographed (silica gel, ethyl acetate/petroleum ether 1:2 to 1:1) to yield 290 mg (44%) desired product as a brown oil.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07569337B2uspto-grants-2009_08