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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003276Generated: October 30, 2026

Trifluoroacetic acid → HCID 53767324, compound

https://huagongshe.com/reaction/1003276

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 dichloromethane (5 ml), a solution of trifluoroacetic acid (5 ml) in dichloromethane (5 ml) was added to the solution under ice-cooling with stirring, and the mixture was still stirred for 15 minutes. After reaction at room temperature for 15 minutes, the reaction mixture was concentrated in vacuo. Dichloromethane, water and sodium bicarbonate were added to the resulting residue and the mixture was stirred at room temperature for 30 minutes. The organic layer was separated and dried over anhydrous magnesium sulfate. The solvent was removed in vacuo to give (S)-4-(2-amino-1,2,3,4-tetrahydronaphthalen-7-yloxy)-N,N-dimethylbutyramide (263 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046192
Source datasetuspto-grants-2000_04
ORD IDord-93291aade2a04a44aa76961a5f9efb91
Source noteuspto-grants-2000_04