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HRID 500070作成日:2026年10月24日

Dimethylformamide → HCID 86629083、化合物

https://huagongshe.com/ja/reaction/500070

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Ammonium ChlorideHCID 25517—
反応物tert-butyl N-(4-oxocyclohexyl)carbamateHCID 1512535—
反応物Potassium tert-butoxideHCID 23665647—
触媒Butyltriphenylphosphonium bromideHCID 159628—
生成物HCID 86629083HCID 86629083—

反応手順

To a mixture of potassium t-butoxide (2.05 g) and anhydrous N,N-dimethylformamide (60 ml) was added butyltriphenylphosphonium bromide (7.30 g) at room temperature. The mixture was stirred for 15 minutes and then a solution of t-butyl 4-oxocyclohexylcarbamate (1.30 g) in N,N-dimethylformamide (10 ml) was added to the mixture. The reaction mixture was stirred at room temperature overnight and then saturated aqueous ammonium chloride was added to the mixture. The mixture was extracted with toluene, and the organic layer was washed with brine, dried over sodium sulfate, and then the solvent was removed in vacuo. After diethyl ether was added to the residue, the precipitate was filtered off and then the filtrate was concentrated under reduced pressure. The residue was purified by a silica gel chromatography (eluent: gradient from 100% hexane/0% ethyl acetate to 0% hexane/100% ethyl acetate) to give 1.40 g of t-butyl (4-butylidenecyclohexyl)carbamate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07767854B2
出典データセットuspto-grants-2010_08
ORD IDord-1fa0f1a583cb4d2886f66a95cb1ac0bd
出典メモuspto-grants-2010_08