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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490133생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/490133

반응식

참여 물질

역할이름HCID투입량
반응물Sodium FluorideHCID 5235—
반응물Potassium CarbonateHCID 11430—
반응물N,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamineHCID 136149—
반응물Tert-butyl (2R,4R)-2-(dimethylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylateHCID 58815374—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물tert-butyl(2R)-2-[(dimethylamino)carbonyl]-4-fluoropyrrolidine-1-carboxylateHCID 69064202—

반응 단계

2.89 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 10 minutes, and under ice cooling, to a suspension of 2.64 g of the compound obtained in step 6-1 and 545 mg of sodium fluoride in 26 mL of dichloromethane, after which the reaction mixture was stirred for 16 hours at room temperature. After this, 100 mL of a 5% potassium carbonate aqueous solution was added under ice cooling to the reaction solution, and the reaction mixture was stirred for 30 minutes at the same temperature. After liquid separation, the aqueous layer thus obtained 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 solvent was distilled off under reduced pressure. The residue thus obtained was subjected to column chromatography (silica gel 60, mobile phase: ethyl acetate) to obtain 2.17 g of the titled compound (colorless solid).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528124B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-338b936ee2b44320b924c4e3d66dcc28
출처 메모uspto-grants-2009_05