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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(cyclohexyl)methyl-7-methoxy-1H-indole | HCID 68701176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(cyclohexyl)methyl-7-methoxy-1H-indole-3-carbaldehyde | HCID 86073288 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700634B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-d0425844a8824adebce6acc1a4d119ae |
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| Source note | uspto-grants-2010_04 |
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