Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21977Generated: October 26, 2026

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

https://huagongshe.com/reaction/21977

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 numberUS05426103
Source datasetuspto-grants-1995_06
ORD IDord-2d71b0967d484a04a693d8513b6e2d68
Source noteuspto-grants-1995_06