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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362574Generated: October 31, 2026

Trifluoroacetic acid → Ethyl (6-aminohexanoyl)aminomethylsalicylate trifluoroacetate

https://huagongshe.com/reaction/362574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactantethyl (N-tert-butoxycarbonyl-6-aminohexanoyl)aminomethylsalicylateHCID 53930957—
SolventDichloromethaneHCID 6344—
ProductEthyl (6-aminohexanoyl)aminomethylsalicylate trifluoroacetateHCID 8675372299%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869623
Source datasetuspto-grants-1999_02
ORD IDord-a79861a59a314a8eaf1a79b457bae12a
Source noteuspto-grants-1999_02