Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711540Generated: October 31, 2026

Triethylamine → HCID 23093475, compound

https://huagongshe.com/reaction/1711540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPivaloyl chlorideHCID 62493—
ReactantN-(tert-Butoxycarbonyl)-N-methyl-2-aminoethanolHCID 545700—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 23093475HCID 23093475—

Reaction Steps

To a mixture of tert-butyl 2-hydroxyethyl(methyl)carbamate (1.75 g) obtained in Reference Example 1 and ethyl acetate (15 mL) was added triethylamine (1.67 mL) and a mixture of trimethylacetyl chloride (1.35 mL), and ethyl acetate (5 mL) was dropwise added. After stirring at room temperature for 2 hrs., pyridine (1.62 mL) was added, and the mixture was stirred overnight at room temperature. Ethyl acetate (50 mL) was added to the reaction mixture, and the mixture was washed with water (50 mL), a 5% aqueous citric acid solution (50 mL) and saturated brine (50 mL), and dried over anhydrous magnesium sulfate. After concentration under reduced pressure, a 4N hydrogen chloride—ethyl acetate solution (10 mL) was added to the residue. After stirring at room temperature for 2 hrs., diethyl ether (10 mL) was added, and the precipitated solid was collected by filtration. The solid was dried under reduced pressure to give the title compound (1.65 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790755B2
Source datasetuspto-grants-2010_09
ORD IDord-94049afc6f1149bba524e6676e829d7d
Source noteuspto-grants-2010_09