戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 392676作成日:2026年10月24日

Trifluoroacetic acid → (2-Trifluoromethyl-7,8-dihydro-3H-6,9-dioxa-1,3-diazacyclopenta[a]naphthalen-8-yl)methyl 4-methylbenzenesulfonate

https://huagongshe.com/ja/reaction/392676

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物[(2R)-7,8-diamino-2,3-dihydro-1,4-benzodioxin-2-yl]methyl 4-methylbenzenesulfonate dihydrochlorideHCID 86586513—
溶媒DichloromethaneHCID 6344—
生成物(2-Trifluoromethyl-7,8-dihydro-3H-6,9-dioxa-1,3-diazacyclopenta[a]naphthalen-8-yl)methyl 4-methylbenzenesulfonateHCID 22341388—

反応手順

A solution of 3.1 g (7.3 mmole) of [(2R)-7,8-diamino-2,3-dihydro-1,4-benzodioxin-2-yl]methyl 4-methylbenzenesulfonate dihydrochloride in 50 mL of trifluoroacetic acid was refluxed under nitrogen for 6 hours. The mixture was diluted to 400 mL with methylene chloride, washed with 400 mL of water and with 400 mL of saturated aqueous sodium bicarbonate, dried over magnesium sulfate, filtered and concentrated to a crude foam in vacuum. The crude product was column chromatographed on silica gel with 1% methanol in chloroform and the product fractions combined and concentrated in vacuum to give 3.3 g of the (R)-enantiomer of the title compound as a white solid (m.p. 114-116° C.), which retains one equivalent of chloroform.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06803368B2
出典データセットuspto-grants-2004_10
ORD IDord-4879152fb38b4a70a3235e3da4bb9941
出典メモuspto-grants-2004_10