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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324648Generated: October 29, 2026

Triethylamine → HCID 22004806, compound

https://huagongshe.com/reaction/324648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium ThiosulfateHCID 24477—
ReactantHCID 10883054HCID 10883054—
SolventDichloromethaneHCID 6344—
ProductHCID 22004806HCID 2200480673%

Reaction Steps

A solution of N-(2-(5-bromo-6-hydroxy-7-(2-methyl-2-propenyl)indan-1-yl)ethyl]propionamide (550 mg, 1.5 mmol.) in dichloromethane (5 mL) was cooled with ice. To the solution were added triethylamine (0.2 mL, 1.5 mmol.) and methachloroperbenzoic acid (1.0 g, 4.1 mmol.). The mixture was stirred for two hours at room temperature. The reaction mixture was poured into an aqueous solution of sodium thiosulfate. The organic matter was extracted with ethyl acetate. The extract solution was washed with 1N HCl and a saturated aqueous solution of sodium hydrogencarbonate, which was then dried over anhydrous magnesium sulfate, followed by distilling off the solvent. The residue was dissolved in dichloromethane, to which was added triethylamine (1 mL). The mixture was stirred for 2 hours at room temperature. The solvent was distilled off under reduced pressure, and the residue was purified by means of silica gel column chromatography (chloroform:methanol=10:1) to afford the title compound (yield 420 mg, 73%) as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218429B1
Source datasetuspto-grants-2001_04
ORD IDord-437a2f3d362845f08df2122020861e66
Source noteuspto-grants-2001_04