HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → Ethyl (6-aminohexanoyl)aminomethylsalicylate trifluoroacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | ethyl (N-tert-butoxycarbonyl-6-aminohexanoyl)aminomethylsalicylate | HCID 53930957 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl (6-aminohexanoyl)aminomethylsalicylate trifluoroacetate | HCID 86753722 | 99% |
Reaction Steps
Ethyl (N-tert-butoxycarbonyl-6-aminohexanoyl)aminomethylsalicylate (0.58 & 1.41 mmoles) was dissolved in dichloromethane (5 mL) and the solution was cooled in an ice/water bath. Trifluoroacetic acid (5 mL) was added, and the reaction was allowed to warm to room temperature. After 2 hours, the reaction mixture was evaporated to dryness to give. the product as an oil, which was dried in vacuo over potassium hydroxide pellets to afford 0. 59 g (99% yield) of ethyl (6-aminohexanoyl)aminomethylsalicylate trifluoroacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05869623 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-a79861a59a314a8eaf1a79b457bae12a |
| Source note | uspto-grants-1999_02 |