戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1410088作成日:2026年10月25日

P-Toluenesulfonamide → 6-Tosyl-2-oxa-6-azaspiro[3.3]heptane

https://huagongshe.com/reaction/1410088

反応式

関与物質

役割名称HCID仕込み量
反応物P-ToluenesulfonamideHCID 6269—
反応物Potassium HydroxideHCID 14797—
反応物Pentaerythritol tribromideHCID 15206—
溶媒EthanolHCID 702—
生成物6-Tosyl-2-oxa-6-azaspiro[3.3]heptaneHCID 2331989169.4%

反応手順

To a solution of KOH (4.98 g, 0.089 mol) and 4-methylbenzenesulfonamide (5.7 g, 0.033 mol) in 90 ml of ethanol, 3-bromo-2,2-bis(bromomethyl)propan-1-ol (9 g, 0.0277 mol) was added at room temperature and the reaction mixture was heated to reflux for 45 h. The solvent was removed by evaporation, 75 ml of 1 M KOH were added and the white suspension was left to stir for another 2 h at room temperature. The mixture was filtered and the white filter cake was rinsed with water until the washing water was neutral. The filter cake was dried under high vacuum to give 4.87 g 6-toluene-4-sulfonyl-2-oxa-6-azaspiro[3.3]heptane (69%) as a white solid. 1H NMR (300 MHz, CDCl3) δ 7.70-7.68 (m, 2H), 7.36-7.34 (m, 2H), 4.58 (s, 4H), 3.90 (s, 4H), 2.45 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08921383B2
出典データセットuspto-grants-2014_12
ORD IDord-18ab945b6bf84d1985df8941b90708f1
出典メモuspto-grants-2014_12