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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533587Generated: November 3, 2026

Trifluoroacetic acid → HCID 86585123, compound

https://huagongshe.com/reaction/1533587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 69623028HCID 69623028—
SolventDichloromethaneHCID 6344—
ProductHCID 86585123HCID 86585123—

Reaction Conditions

Temperature0 °C

Reaction Steps

(S)-2-(tert-Butoxycarbonylamino)-2-(6-methoxy-2-naphthyl)acetic acid was then converted into the methyl ester using General Procedure G below. The methyl ester was then dissolved in CH2Cl2 and this solution cooled to 0° C. Trifluoroacetic acid (50 molar eq.) was added and the reaction was allowed to warm to room temperature and stirring was continued for 2 hrs. The reaction mixture was then concentrated and the residue extracted into CH2Cl2 and washed with sodium bicarbonate solution. The organic layer was dried over Na2SO4, filtered and concentrated to yield methyl (S)-2-amino-2-(6-methoxy-2-naphthyl)acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06207710B1
Source datasetuspto-grants-2001_03
ORD IDord-a36e729804424513b1a2d4b9c0e6bf7f
Source noteuspto-grants-2001_03