반응식
[O-]CC.[Na+].[NH2:5][CH:6]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:7]([O:9][CH2:10][CH3:11])=[O:8].Br[CH2:18][CH2:19][CH2:20]Br>C(O)C.Cl>[NH:5]1[CH2:20][CH2:19][CH2:18][C:6]1([C:7]([O:9][CH2:10][CH3:11])=[O:8])[C:12]([O:14][CH2:15][CH3:16])=[O:13]참가 물질
실험 절차
To a solution of sodium ethoxide (5.14 g) in absolute ethanol (75 mL) at 0° C. under a nitrogen atmosphere, a solution of diethyl aminomalonate (hydrochloride salt, 8 g) in absolute ethanol (75 mL) was slowly added. A yellow suspension was obtained at the end of the addition. 1,3-dibromo propane (7.7 mL) was then added and the resulting mixture was stirred at reflux temperature for 5 hours. The mixture was allowed to cool down to rt, then ethanol was removed in vacuo to give a yellow solid. This was dissolved in HCl (1M solution, 20 mL) and then washed with ethyl ether (2×50 mL). Phases were separated and the aqueous phase was brought to pH=9 by adding NaOH (1M solution). It was then extracted with ethyl ether (3×50 mL) and washed with brine (20 mL). The organic phase was dried and concentrated in vacuo to give the desired compound (2.35 g) as yellow oil.
후처리
- customA yellow suspension was obtained at the end of the addition
- temperatureat reflux temperature for 5 hours
- customethanol was removed in vacuo
- customto give a yellow solid
- washwashed with ethyl ether (2×50 mL)
- customPhases were separated
- additionby adding NaOH (1M solution)
- extractionIt was then extracted with ethyl ether (3×50 mL)
- washwashed with brine (20 mL)
- customThe organic phase was dried
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-4fa3026d12d047dbbd6729e9420bc257
- 출처 데이터셋
- uspto-grants-2012_01
- 특허 번호
- US08097618B2
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