HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399265Generated: October 30, 2026
Trifluoroacetic anhydride → 5-Chloro-6-(2-dimethylaminoethoxy)-1H-indole
https://huagongshe.com/reaction/399265
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-[4-Chloro-3-(2-dimethylaminoethoxy)phenyl]aminoacetaldehyde dimethyl acetal | HCID 57027129 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 5-Chloro-6-(2-dimethylaminoethoxy)-1H-indole | HCID 54086422 | 77.5% |
Reaction Steps
A solution of N-[4-chloro-3-(2-dimethylaminoethoxy)phenyl]aminoacetaldehyde dimethyl acetal (D7, 0.61 g, 0.002 mol) in TFA (2.6 ml) at 0° C., was treated with TFAA (2.6 ml) under an argon atmosphere. More TFA (3.7 ml ) was added and the reaction was heated to reflux for 48 h. The solution was evaporated to dryness and the residue taken up in EtOAc. The extract was dried (Na2SO4) and concentrated in vacuo to leave a brown oil which was dissolved in MeOH (10 ml), treated with K2CO3 (1 g) and then stirred at room temperature for 3 h The mixture was concentrated in vacuo, and then the residue treated with water and extracted with EtOAc. The solution was dried (Na2SO4) and concentrated in vacuo to give the title compound as a brown solid (0.37 g , 76%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05817833 |
|---|
| Source dataset | uspto-grants-1998_10 |
|---|
| ORD ID | ord-9226eaef93244376b2c927ac898b39ae |
|---|
| Source note | uspto-grants-1998_10 |
|---|