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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715248Generated: November 2, 2026

Triethylamine → HCID 131728332, compound

https://huagongshe.com/reaction/1715248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-2-methyl-1-propanolHCID 11807—
ReactantN-((1,1-dimethylethoxy)carbonyl)-beta-alanineHCID 76809—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
SolventDichloromethaneHCID 6344—
SolventCyclohexane ethylacetateHCID 21867204—
ProductHCID 131728332HCID 131728332127%

Reaction Steps

To a mixture of 2-amino-2-methyl-1-propanol (177.4 mg; 1.99 mmol; 1 eq) and boc-beta-alanine (338.9 mg; 1.79 mmol; 0.9 eq) in DCM (30 ml), are added triethylamine (0.83 ml; 5.97 mmol; 3 eq) and 2-chloro-1-methylpyridinium iodide (1525 mg; 5.97 mmol; 3 eq). The mixture is stirred for 2 days at RT. The reaction is followed by TLC (cyclohexane/EtOAc 1:1). The reaction mixture is then washed twice with NH4Cl sat. solution and twice with NaHCO3 sat. solution. The organic layer is dried over Na2SO4, filtered and concentrated to give 592 mg of an orange oil, which is purified by flash chromatography (cyclohexane/EtOAc gradient, from 9/1 to 1/1 over 30 min). The title compound is isolated as a slightly yellow solid (331.1 mg; 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799814B2
Source datasetuspto-grants-2010_09
ORD IDord-c39fbd2c59944ca68c55d766df362032
Source noteuspto-grants-2010_09