HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 3-(trifluoroacetyl)-1H-indole-1-ylmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 3-(Trifluoroacetyl)indole | HCID 589126 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-(trifluoroacetyl)-1H-indole-1-ylmethanol | HCID 23149193 | 97.9% |
Reaction Conditions
| Temperature | 130 °C |
|---|
Reaction Steps
The mixture of 4.80 g of 3-(trifluoroacetyl)-1H-indole, 1.35 g of paraformaldehyde and 0.10 g of triethylamine was stirred at 130° C. for 2 hours. After the reaction mixture was cooled to room temperature, acetone was added to the reaction mixture. The mixture was filtered, and then the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography, and hexane was added to the residue, as a result, a crystal was formed. The crystal was collected to obtain 5.36 g of 3-(trifluoroacetyl)-1H-indole-1-ylmethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07541374B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-c0833845bd4d4bfc98159442bc2ddafb |
| Source note | uspto-grants-2009_06 |