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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359472Generated: November 1, 2026

Triethylamine → HCID 69111269, compound

https://huagongshe.com/reaction/1359472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
ReactantHCID 22145244HCID 22145244—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 69111269HCID 6911126918%

Reaction Steps

A mixture of racemic 5-isopropoxy-2-aminotetraline-2-carboxylic acid (3.48 g, 5.98 mmole theoretical), triethylamine (1.10 ml, 7.89 mmole), 9-fluorenylmethyl succinimidyl carbonate (Fmoc-OSu, 2.62 g, 7.77 mmole) in acetonitrile (30 ml) and water (30 ml) was stirred at room temperature for one day. TLC analysis of the reaction indicated the presence of starting material amino acid. 9-fluorenylmethyl succinimidyl carbonate (500 mg) 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 methylene chloride. 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 1→2→5→8% methanol/methylene chloride) to give racemic Fmoc-5-isopropoxy-2-aminotetraline-2-carboxylic acid (0.50 g, 18% yield over 2 steps) as a white solid. HRMS (FAB): C29H30NO5 (M+H) calc. 472.2124; observed: 472.2117.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06600015B2
Source datasetuspto-grants-2003_07
ORD IDord-c33efdb909694fdf8b588aba3bd80941
Source noteuspto-grants-2003_07