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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53143생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/53143

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
반응물5-NitroindoleHCID 22523—
촉매L-ProlineHCID 145742—
용매AcetonitrileHCID 6342—
생성물5-(5-Nitroindol-3-ylmethyl)-2,2-dimethyl-1,3-dioxane4,6-dioneHCID 1522826381%

반응 단계

An adaption of the procedure of Flaugh1 was used. Thus, a solution of 5-nitroindole (50.0 g, 0.32 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, mp 182° C. (dec). The mother liquor was concentrated and then diluted with H2O, and the resulting solid was collected, washed and dried as before to give a second crop of the product (7.0 g) as a darker yellow solid. Total yield=87.0 g (89%): IR (KBr) 3330, 1767, 1732 cm-1 ; 1H NMR (DMSO-d6, 200 MHz) δ11.64 (s, 1H), 8.63 (d, J=2.2 Hz, 1H), 7.96 (dd, J=9.0, 2.2 Hz, 1H), 7.49 (d, J=9.0 Hz, 1H), 7.33 (d, J=2.2 Hz, 1H), 4.84 (t, J=4.6 Hz, 1H), 3.45 (d, J=4.5 Hz, 2H), 1.78 (s, 3H), 1.55 (s, 3H). Anal. Calcd for C15H14N2O6 : C, 56.60; H, 4.43; N, 8.80. Found: C, 56.62; H, 4.41; N, 8.91.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05618816
출처 데이터셋uspto-grants-1997_04
ORD IDord-ee9fddc37b7c426e95202c33d76ad144
출처 메모uspto-grants-1997_04