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HRID 491903Erstellt: 25. Oktober 2026

2,2-Dimethyl-1,3-dioxane-4,6-dione → (R)-[1-(2,2-Dimethyl-4,6-dioxo-[1,3]dioxane-5-carbonyl)-2-methyl-propyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/491903

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 16249—
Edukt(2R)-2-(((tert-butoxy)carbonyl)amino)-3-methylbutanoic acidHCID 637605—
LösungsmittelDichloromethaneHCID 6344—
Produkt(R)-[1-(2,2-Dimethyl-4,6-dioxo-[1,3]dioxane-5-carbonyl)-2-methyl-propyl]-carbamic acid tert-butyl esterHCID 58856323—

Reaktionsbedingungen

Temperatur3 °C

Reaktionsschritte

A 5 L four-necked flask (equipped with mechanical stirrer, nitrogen inlet, thermocouple, and glass stopper) was charged with Boc-D-Valine (143.6 g, 0.661 mol) and dichloromethane (2.8 L). The reaction was chilled to ˜3° C. in an ice bath, and then 4-N,N-dimethylaminopyridine (124.6 g, 1.02 mol) and Meldrum's acid (104.8 g, 0.727 mol) were added to the reaction. To the reaction mixture was then added 1-[3-(dimethylaminopropyl)]-3-ethylcarbodiimide hydrochloride (EDCl, 139.4 g, 0.727 mol) over a five-minute period, and then the reaction mixture was allowed to warm to room temperature over 18 h (overnight). The reaction mixture washed with 5% (w/w) aqueous potassium bisulfate (4×600 mL), dried (MgSO4), and the solution was used directly in the next step without concentration or purification. A small portion was concentrated and displayed the following analytical data.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07531545B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-d74dd21795f34a61bd3ea70a079ed615
Quellennotizuspto-grants-2009_05