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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825267Generated: November 2, 2026

Triethylamine → HCID 69109997, compound

https://huagongshe.com/reaction/1825267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
ReactantHCID 22145259HCID 22145259—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 69109997HCID 69109997107.9%

Reaction Steps

A mixture of racemic 5-ethoxy-2-aminotetraline-2-carboxylic acid (2.22 g, 9.44 mmole), triethylamine (2.00 ml, 14.3 mmole), 9-fluorenylmethyl succinimidyl carbonate (Fmoc-OSu, 4.81 g, 14.3 mmole) in acetonitrile (75 ml) and water (75 ml) was stirred at room temperature for two days. TLC analysis of the reaction indicated the presence of starting material amino acid. 9-fluorenylmethyl succinimidyl carbonate (645 mg) and triethylamine (1.0 ml) was added and the mixture was stirred at room temperature for another day. The reaction mixture was concentrated in vacuo to remove most of the acetonitrile, acidified to pH 3 with 10% aqueous citric acid solution, and the white emulsion extracted three times with ethyl acetate. The combined organic layers were washed with water, brine, dried over magnesium sulfate. Filtration and concentration gave a crude oil which was purified by column chromatography (eluted with 3→5→10% methanol/methylene chloride) to give racemic Fmoc-5-ethoxy-2-aminotetraline-2-carboxylic acid (4.66 g, >quantitative yield) as a white solid. HRMS (FAB): C28H28NO5 (M+H) calc. 458.1967; observed: 458.1985.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045591B2
Source datasetuspto-grants-2006_05
ORD IDord-7cf4df7a7d9f4c2d9e39bb6fca5ac947
Source noteuspto-grants-2006_05