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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490121생성일: 2026년 10월 24일

Sodium Fluoride → tert-butyl(2S,4R)-2-[(dimethylamino)carbonyl]-4-fluoropyrrolidine-1-carboxylate

https://huagongshe.com/ko/reaction/490121

반응식

참여 물질

역할이름HCID투입량
반응물Sodium FluorideHCID 5235—
반응물N,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamineHCID 136149—
반응물Sodium BicarbonateHCID 516892—
반응물tert-butyl (2S,4S)-2-(dimethylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylateHCID 67430109—
용매DichloromethaneHCID 6344—
용매Ethyl acetate hexaneHCID 21226206—
생성물tert-butyl(2S,4R)-2-[(dimethylamino)carbonyl]-4-fluoropyrrolidine-1-carboxylateHCID 67428750—

반응 단계

8.85 g of a mixture (approximately 3:1) of 1,1,2,3,3,3-hexafluoro-1-(diethylamino)propane and 1,2,3,3,3-pentafluoro-1-(diethylamino)-2-propene was added dropwise over a period of 2 minutes under ice cooling to a suspension of 8.54 g of the compound obtained in step 1-1b and 1.67 g of sodium fluoride in 90 mL of dichloromethane, after which the reaction mixture was stirred for 15 hours at room temperature. 200 mL of a saturated sodium hydrogencarbonate aqueous solution was added dropwise to the reaction solution over a period of 3 minutes, and the reaction mixture was stirred for 1 hour. After liquid separation, the aqueous layer was extracted with chloroform (30 mL×2), and the combined organic layer was washed with 50 mL of saturated brine and dried with magnesium sulfate, after which the drying agent was filtered off and the reaction mixture was concentrated under reduced pressure. The residue thus obtained was subjected to column chromatography (silica gel 60, mobile phase: ethyl acetate/n-hexane=1/1 to 10/0; v/v) to obtain 7.54 g of the titled compound (pale yellow solid).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528124B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-4b4ebc80d4454c65a2ab4a904986eab6
출처 메모uspto-grants-2009_05