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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003274Generated: October 30, 2026

HCID 53730197, compound → HCID 54067144, compound

https://huagongshe.com/reaction/1003274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 53730197HCID 53730197—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventSodium HydroxideHCID 14798—
ProductHCID 54067144HCID 5406714499.9%

Reaction Steps

Ethyl (s)-4-[2-(tert-butoxycarbonylamino)-1,2,3,4-tetra-hydronaphthalen-7-yloxy]butyrate (988 mg) was dissolved in a mixed solvent of methanol (15 ml) and ethanol (15 ml), and 2N aqueous sodium hydroxide solution (3.0 ml) was added to the solution at room temperature with stirring. After reaction for 2 hours, the reaction mixture was concentrated in vacuo. To the resulting residue was added 10% aqueous citric acid solution, and the mixture was extracted with ethyl acetate. The extract was washed with brine and dried over anhydrous magnesium sulfate. The solvent was removed in vacuo to give (S)-4-[2-(tert-butoxycarbonylamino)-1,2,3,4-tetrahydronaphthalen-7-yloxy]butyric acid (914 mg) having a melting point of 150-153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046192
Source datasetuspto-grants-2000_04
ORD IDord-5fc4caa8960346e2b251f910ba5d3695
Source noteuspto-grants-2000_04