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HRID 490119作成日:2026年10月26日

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

https://huagongshe.com/reaction/490119

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium FluorideHCID 5235—
反応物Potassium CarbonateHCID 11430—
反応物N,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamineHCID 136149—
反応物(2S,4R)-tert-butyl 2-(dimethylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylateHCID 25180889—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl acetate hexaneHCID 21226206—
生成物tert-butyl(2S,4R)-2-[(dimethylamino)carbonyl]-4-fluoropyrrolidine-1-carboxylateHCID 67428750—

反応手順

26.6 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 under ice cooling to a suspension of 25.7 g of the compound obtained in step 1-1a and 5.00 g of sodium fluoride in 260 mL of dichloromethane, after which the reaction mixture was stirred for 16 hours at room temperature. 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, 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/n-hexane=1/1 to 10/0; v/v) to obtain 12.2 g of the titled compound (pale yellow solid).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07528124B2
出典データセットuspto-grants-2009_05
ORD IDord-7a5cfd9f7de94b12a9f824563214f085
出典メモuspto-grants-2009_05