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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825265Generated: November 1, 2026

Triethylamine → HCID 69110274, compound

https://huagongshe.com/reaction/1825265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
ReactantHCID 22145234HCID 22145234—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 69110274HCID 6911027471%

Reaction Steps

A mixture of racemic 5-methoxy-2-aminotetraline-2-carboxylic acid (prepared according to Obrecht, D. et. al. Helv. Chim Acta. 1992, 75, 1666) (802 mg, 3.62 mmole), triethylamine (0.62 ml, 4.45 mmole), 9-fluorenylmethyl succinimidyl carbonate (Fmoc-OSu, 1.47 g, 4.36 mmole) in acetonitrile (25 ml) and water (25 ml) was stirred at room temperature for 30 hours. TLC analysis of the reaction indicated the presence of starting material amino acid. 9-fluorenylmethyl succinimidyl carbonate (370 mg) and triethylamine (0.6 ml) were added and the mixture was stirred at room temperature for another 24 hours. 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 was extracted three times with ethyl acetate. The combined organic layers were washed with water, brine and dried over magnesium sulfate. Filtration and concentration gave a crude oil which was purified by column chromatography (eluted with 1→3→5→10% methanol/methylene chloride) to give racemic Fmoc-5-methoxy-2-aminotetraline-2-carboxylic acid (1.14 g, 71% yield) as an off-white solid. HRMS (FAB): C27H26NO5 (M+H) calc. 444.1812; observed: 444.1814.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045591B2
Source datasetuspto-grants-2006_05
ORD IDord-20f275d695e94ed5a34f716a2736062f
Source noteuspto-grants-2006_05