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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367327Generated: October 30, 2026

Trifluoroacetic acid → HCID 53767324, compound

https://huagongshe.com/reaction/367327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 21967812HCID 21967812—
SolventDichloromethaneHCID 6344—
ProductHCID 53767324HCID 5376732490.5%

Reaction Steps

(S)-4-[2-(tert-Butoxycarbonylamino)-1,2,3,4-tetrahydronaphthalen-7-yloxy]-N,N-dimethylbutyramide (396 mg) was dissolved in 5 ml of methylene chloride, a solution of 5 ml of trifluoroacetic acid in 5 ml of methylene chloride was added to the solution with stirring under ice-cooling, and the mixture was stirred for 15 minutes and then subjected to 15 minutes of reaction at room temperature. The reaction solution was concentrated under reduced pressure, methylene chloride, water and sodium bicarbonate were added to the residue, and the mixture was stirred at room temperature for 30 minutes. The organic layer was separated and dried over anhydrous magnesium sulfate. By evaporating the solvent under reduced pressure, 263 mg of (S)-4-(2-amino-1,2,3,4-tetrahydronaphthalen-7-yloxy)-N,N-dimethylbutyramide was obtained in an oily form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133266
Source datasetuspto-grants-2000_10
ORD IDord-fd0fe41568954a62885455a1ee27705a
Source noteuspto-grants-2000_10