Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154538Generated: October 31, 2026

Tetrahydrofuran → HCID 18772239, compound

https://huagongshe.com/reaction/1154538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantGlycine, N-2-naphthalenyl-HCID 457448—
ReactantCarbonic acid, bis(1,1-dimethylethyl) esterHCID 10219638—
SolventSodium HydroxideHCID 14798—
ProductHCID 18772239HCID 1877223985.5%

Reaction Conditions

Temperature24 °C

Reaction Steps

To a stirred solution of 10 g (50 mM) of 2-naphthylglycine (from Preparation 1) in 100 ml of 1N sodium hydroxide were added 50 ml of tetrahydrofuran followed by 30 g (140 mM) of di-tert.-butyl carbonate. The reaction mixture was stirred at 24° C. for four hours. The product was isolated by first washing the reaction mixture three times with 50 ml portions of diethyl ether, and then the mixture was made acidic to pH 2.0 by the addition of conc. hydrochloric acid. The aqueous acid mixture was extracted several times with ethyl acetate, and the extracts were combined, washed with water, dried and the solvent was removed by evaporation under reduced pressure to provide 12.8 g (85% yield) of N-tert.-butoxycarbonyl-2-naphthylglycine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04490370
Source datasetuspto-grants-1984_12
ORD IDord-fb1c5794a7884e4e86f87f256ab11b37
Source noteuspto-grants-1984_12