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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644068Generated: October 30, 2026

Dimethylformamide → 1-(cyclohexyl)methyl-7-methoxy-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/644068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(cyclohexyl)methyl-7-methoxy-1H-indoleHCID 68701176—
SolventWaterHCID 962—
Product1-(cyclohexyl)methyl-7-methoxy-1H-indole-3-carbaldehydeHCID 86073288—

Reaction Conditions

Temperature0 °C

Reaction Steps

Phosphorous oxychloride (12 ml, 0.13 mol) was added slowly over 30 minutes to dimethylformamide (30 ml) at −10° C. The solution was allowed to warm to 0° C. over 1 h, then 1-(cyclohexyl)methyl-7-methoxy-1H-indole (prepared as in Example 26; 3.2 g, 13 mmol) was added portionwise and the solution stirred at room temperature for 16 h. The solution was cooled in an ice bath and diluted with water, then neutralised carefully with sodium bicarbonate and extracted with ethyl acetate (3×50 ml). The organic extracts were combined and the solvent removed in vacuo. The residue (3.5 g) was dissolved in aqueous sodium hydroxide solution (5 M; 100 ml) and the mixture refluxed at 100° C. for a further 16 h. The solution was cooled and extracted with ethyl acetate (3×50 ml), the organic extracts combined and the solvent removed in vacuo to afford 1-(cyclohexyl)methyl-7-methoxy-1H-indole-3-carbaldehyde (2.2 g, 8.12 mmol) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700634B2
Source datasetuspto-grants-2010_04
ORD IDord-d0425844a8824adebce6acc1a4d119ae
Source noteuspto-grants-2010_04