HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338446Generated: October 29, 2026
Dimethylformamide → 6-Chloro-5-(4-(2-hydroxyethyl)-3-methoxyphenyl)-1h-indole-3-carbaldehyde
https://huagongshe.com/reaction/338446
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Chloro-N,N-dimethylformiminium chloride | HCID 77311 | — |
| Reactant | 2-(4-Bromo-2-methoxyphenyl)ethanol | HCID 66580015 | — |
| Reactant | 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole | HCID 86698733 | — |
| Product | 6-Chloro-5-(4-(2-hydroxyethyl)-3-methoxyphenyl)-1h-indole-3-carbaldehyde | HCID 86698777 | — |
Reaction Steps
To a 0.4M solution of chlormethylene dimethylammonium chloride in DMF (7.5 mL, 3.8 mmol) was added 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole (493 mg, 1.88 mmol). The mixture was stirred at 30° C. for 2 hrs. 0.50 mL of this solution (0.15 mmol) was placed in a vial with a 0.3M solution of 2-(4-bromo-2-methoxyphenyl)ethanol in DMF (0.50 mL, 0.15 mmol). 2M potassium carbonate (0.30 mL, 0.60 mmol) was then added and the mixture was purged with nitrogen. PddppfCl2 (9 mg, 0.01 mmol) was then added and the vial capped and heated to 90° C. for 3 hours. The reaction mixture was concentrated by Speedvac and purified via preparative TLC to give the title compound that was taken forward without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889730B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-7ca502a1c01a4f7a9dbad1828c355557 |
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| Source note | uspto-grants-2014_11 |
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