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HRID 341770생성일: 2026년 10월 27일

Hydrochloric Acid → 1-tert-Butyl 3-ethyl 4-oxopyrrolidine-1,3-dicarboxylate

https://huagongshe.com/reaction/341770

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl AcrylateHCID 8821—
반응물Benzenesulfonic acid, 4-(2-(4-(dimethylamino)phenyl)diazenyl)-HCID 11037—
반응물Sodium hydrideHCID 24758—
반응물Ethyl 2-((tert-butoxycarbonyl)amino)acetateHCID 357729—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물1-tert-Butyl 3-ethyl 4-oxopyrrolidine-1,3-dicarboxylateHCID 1086894271%

반응 단계

To a refluxing suspension of 1.58 g (66 mmol) sodium hydride in 100 ml THF was added dropwise a solution of 12.79 g (60 mmol) N-tert-butyloxycarbonyl-glycine ethyl ester and 7.15 g (66 mmol) ethyl acrylate in 100 ml THF. After the addition was complete the mixture was heated to reflux for additional 2 h. The clear solution was cooled to room temperature, poured on 100 ml ether/100 ml water and acidified under vigorous stirring with 1N hydrochloric acid against methyl orange. The layers were separated and the aqueous layer was extracted three times with ether. The combined organic layers were washed with sat. sodium bicarbonate and brine, dried over MgSO4 and evaporated. Short-path distillation of the residue gave 10.92 g (71%) 4-oxo-pyrrolidine-1,3-dicarboxylic acid 1-tert. butylester 3-ethylester as a colorless oil, b.p. 119°-122° C. (0.2 mbar), which solidified on prolonged standing in the freezer.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05856309
출처 데이터셋uspto-grants-1999_01
ORD IDord-465369b8f60c46f9bab61dbad1988d8b
출처 메모uspto-grants-1999_01