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HRID 421205作成日:2026年10月27日

1,3-Dibromopropane → Diethyl 2,2-pyrrolidinedicarboxylate

https://huagongshe.com/reaction/421205

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-DibromopropaneHCID 8001—
反応物Propanedioic acid, 2-amino-, 1,3-diethyl esterHCID 81272—
反応物Sodium ethoxideHCID 2723922—
溶媒Hydrochloric AcidHCID 313—
溶媒EthanolHCID 702—
生成物Diethyl 2,2-pyrrolidinedicarboxylateHCID 12524347—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08097618B2
出典データセットuspto-grants-2012_01
ORD IDord-4fa3026d12d047dbbd6729e9420bc257
出典メモuspto-grants-2012_01