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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647788Generated: October 25, 2026

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

https://huagongshe.com/reaction/1647788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
Reactant5-NitroindoleHCID 22523—
ReactantL-ProlineHCID 145742—
SolventAcetonitrileHCID 6342—
Product5-(5-Nitroindol-3-ylmethyl)-2,2-dimethyl-1,3-dioxane4,6-dioneHCID 1522826381.1%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05434154
Source datasetuspto-grants-1995_07
ORD IDord-af33cdcee8c04c808c2bc21313a031c2
Source noteuspto-grants-1995_07