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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825264Generated: October 31, 2026

Triethylamine → HCID 69110373, compound

https://huagongshe.com/reaction/1825264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
ReactantHCID 22145240HCID 22145240—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 69110373HCID 6911037368%

Reaction Steps

A mixture of racemic 5-chloro-2-aminotetraline-2-carboxylic acid (402 mg, 1.78 mmole), triethylamine (0.38 ml, 2.73 mmole), 9-fluorenylmethyl succinimidyl carbonate (Fmoc-OSu, 904 mg, 2.68 mmole) in acetonitrile (20 ml) and water (20 ml) was stirred at room temperature for two days. TLC analysis of the reaction after two days indicated the presence of starting material amino acid. 9-fluorenylmethyl succinimidyl carbonate (0.12 g) and triethylamine (0.1 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→6→8% methanol/methylene chloride) to give racemic Fmoc-5-chloro-2-aminotetraline-2-carboxylic acid (540 mg, 68% yield) as a white solid. HRMS (EI): C26H22ClNO4 (M) calc. 447.1237; observed: 447.1234.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045591B2
Source datasetuspto-grants-2006_05
ORD IDord-57fa7fda1f77402ba6899df5d6abbe4f
Source noteuspto-grants-2006_05