HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 5-[4-(1-Methylindolin-2-ylmethoxy)benzyl]thiazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 5-[4-(1-Methylindolin-2-ylmethoxy)benzyl]-3-triphenylmethylthiazolidine-2,4-dione | HCID 23298359 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-[4-(1-Methylindolin-2-ylmethoxy)benzyl]thiazolidine-2,4-dione | HCID 15435852 | 79.6% |
Reaction Steps
3.1 ml of trifluoroacetic acid were added to a solution of 2.50 g of 5-[4-(1-methylindolin-2-yl-methoxy)benzyl]-3-triphenylmethylthiazolidine-2,4-dione (prepared as described in Preparation 7) in 25 ml of methylene chloride, and the resulting mixture was stirred at room temperature for 1 hour. At the end of this time, the reaction mixture was worked up following the procedure described in Example 1, to give 1.20 g of the title compound, melting at 46.1°-48.9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05834501 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-91bb921297624ec5a5fec602d1a698e9 |
| Source note | uspto-grants-1998_11 |