HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → (2-tert-butyl-6-nitro-1H-indol-3-yl)-acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-tert-butyl-3-(2,2-dimethoxy-ethyl)-6-nitro-1H-indole | HCID 57899234 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2-tert-butyl-6-nitro-1H-indol-3-yl)-acetaldehyde | HCID 57899287 | 91.6% |
Reaction Steps
To a solution of 2-tert-butyl-3-(2,2-dimethoxy-ethyl)-6-nitro-1H-indole (0.80 g, 2.6 mmol) in methylene chloride (10 mL) was added trifluoroacetic acid (5 mL, 50%) at 0° C. and the resulting solution was stirred at room temperature for 6 h. Saturated sodium bicarbonate was added until pH>7. The aqueous layer was extracted with methylene chloride several times. The combined organic layers were dried over sodium sulfate, filtrated, and concentrated in vacuo. The residue was purified via silica gel column chromatography to give the title compound (0.62 g, 91%). LCMS (m/z): 261.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943652B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-cf81f38d407240e19865290ee61cab7c |
| Source note | uspto-grants-2011_05 |