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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1647788생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1647788

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
반응물5-NitroindoleHCID 22523—
반응물L-ProlineHCID 145742—
용매AcetonitrileHCID 6342—
생성물5-(5-Nitroindol-3-ylmethyl)-2,2-dimethyl-1,3-dioxane4,6-dioneHCID 1522826381.1%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05434154
출처 데이터셋uspto-grants-1995_07
ORD IDord-af33cdcee8c04c808c2bc21313a031c2
출처 메모uspto-grants-1995_07