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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954826Generated: November 3, 2026

Triethylamine → HCID 53996705, compound

https://huagongshe.com/reaction/1954826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Butoxybenzoic acidHCID 72971—
ReactantHCID 54282228HCID 54282228—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
SolventThionyl ChlorideHCID 24386—
ProductHCID 53996705HCID 53996705—

Reaction Steps

4-Butoxybenzoic acid (0.16 g, 0.8 mmol) was dissolved in thionyl chloride (3 mL) and refluxed for 30 minutes. The excess of thionyl chloride was removed in vacuo with toluene. The residue was dissolved in methylene chloride (5 mL) and added dropwise to an ice cold solution of (R)-2-amino-8-(1-methylpiperidin-4-yl)-1,2,3,4-tetrahydronaphthalene (0.15 g, 0.6 mmol) and triethylamine (92 mg, 0.9 mmol) in methylene chloride (5 mL). The mixture was stirred for 30 minutes and was then diluted with ethyl acetate, washed with ammonia (2 is M) and dried (MgSO4). The solvent was removed in vacuo. The residue was purified by flash chromatography on silica gel using methylene chloride/ethanol 5:1, containing 0.5% of ammonia, as the eluent. The title compound was obtained as white crystals. Yield 170 mg (50%): mp 162-164° C.; [α]21D -2° (c 0.5, CHCl3); EIMS (70 eV) m/z (relative intensity) 420 (40, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124283
Source datasetuspto-grants-2000_09
ORD IDord-a16fcc2d444c46a1be3e96c2adad1561
Source noteuspto-grants-2000_09