戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 68221作成日:2026年10月25日

Potassium Carbonate → tert-Butyl 3-oxocyclobutylcarbamate

https://huagongshe.com/reaction/68221

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物tert-butyl N-(3-methylidenecyclobutyl)carbamateHCID 28875369—
触媒Tetrabutylammonium ChlorideHCID 70681—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物tert-Butyl 3-oxocyclobutylcarbamateHCID 23374584177.6%

反応手順

To a vigorously stirring solution of N-Boc-3-methylene-cyclobutanamine (9.8 g, 53.5 mmol) in DCM (160 mL) and H2O (160 mL) was added K2CO3 (3 g, 21.7 mmol), followed by NaClO4 (35 g, 163.5 mmol), tetrabutylammonium chloride (0.2 g, 0.72 mmol) and RuCl3 (0.6 g, 7.6 mmol). During the course of the reaction, the organic solution turned dark brown, the catalyst turned black, while the upper aqueous layer turned white. The reaction was monitored by TLC, and upon completion, the reaction mixture was filtered through a pad of celite. The filtrates were transferred to a separatory funnel, and the aqueous layer was extracted with DCM (2×50 mL). The combined organic layers were washed with 5% NaHCO3 (2×30 mL), brine (30 mL), dried over Na2SO4, filtered and evaporated to dryness to yield a crude, which was purified by flash chromatography (silica gel/hexanes:ethyl acetate 0-60%) to yield the desired N-Boc-3-amino-cyclobutanone (7.13 g, 38.53 mmol, 72% yield): NMR (250 MHz, CDCl3) δ 4.88 (bs, 1H), 4.13-4.29 (m, 1H), 3.23-3.41 (m, 2H), 2.9-3.05 (m, 2H), 1.39 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822424B2
出典データセットuspto-grants-2014_09
ORD IDord-44c9661632504064abfdcf13d1a6d774
出典メモuspto-grants-2014_09