Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5404Generated: October 24, 2026

Triethylamine → 10-(Acetylthiomethyl)-3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane

https://huagongshe.com/en/reaction/5404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Thiopheneacetic acidHCID 15970—
Reactant2-Fluoro-1-methylpyridinium p-toluenesulfonateHCID 171631—
Reactant3-t-Butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecaneHCID 19930843—
SolventAcetoneHCID 180—
SolventBenzeneHCID 241—
Product10-(Acetylthiomethyl)-3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecaneHCID 19930829—

Reaction Steps

3-t-Butoxycarbonylmethyl-10-hydroxymethyl-2-oxo-1-azacyclodecane (0.50 g, 1.67 mmol) is dissolved in acetone (5.0 mL) and benzene (5.0 mL). Triethylamine (0.26 mL, 1.9 mmol) is added, followed by 2-fluoro-1-methylpyridinium toluene-4-sulfonate (0.54 g, 1.9 mmol), and the reaction is stirred at room temperature for 90 minutes. Thiolacetic acid (0.14 mL, 1.9 mmol) and more triethylamine (0.26 mL, 1.9 mmol) are added, and the reaction is heated to reflux for 2 hours. The solvent is then removed, the crude product is partitioned between methylene chloride and water, and the aqueous phase is extracted several times with methylene chloride. The combined organic layers are dried (MgSO4) and the solvent is evaporated. The crude product is purified by silica gel chromatography (15% ethyl acetate/hexane) to give 10-(acetylthiomethyl)-3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane, MS: M+1=358.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244889
Source datasetuspto-grants-1993_09
ORD IDord-b0cbfac023104194ba68e11d16883fb1
Source noteuspto-grants-1993_09