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HRID 1647788作成日:2026年10月26日

Formaldehyde → 5-(5-Nitroindol-3-ylmethyl)-2,2-dimethyl-1,3-dioxane4,6-dione

https://huagongshe.com/reaction/1647788

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
反応物5-NitroindoleHCID 22523—
反応物L-ProlineHCID 145742—
溶媒AcetonitrileHCID 6342—
生成物5-(5-Nitroindol-3-ylmethyl)-2,2-dimethyl-1,3-dioxane4,6-dioneHCID 1522826381.1%

反応手順

An adaption of the procedure of Flaugh1 was used. Thus, a solution of 5-nitroindole (50.0 g, 0.31 mol), Meldrum's acid (46.0 g, 0.32 mol), 37% aqueous formaldehyde (26.0 mL, 0.32 mol) and proline (1.8 g, 0,016 mol) in 200 mL of acetonitrile was stirred at room temperature for 18 h. The resulting thick yellow slurry was filtered and the filtercake was washed with acetonitrile, then acetone and finally with ether. This material was dried in vacuo to give the title compound (80.0 g, 81%) as a bright yellow solid, m.p. 182° C. (dec). The mother liquor was concentrated and then diluted with H2O, and the resulting solid was collected and washed and dried as before. This gave a second crop of the product (7.0 g) as a darker yellow solid. Total yield=87.0 g (89%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05434154
出典データセットuspto-grants-1995_07
ORD IDord-af33cdcee8c04c808c2bc21313a031c2
出典メモuspto-grants-1995_07