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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 747800Erstellt: 24. Oktober 2026

Methanol → Methyl 3-azido-2-hydroxypropionate

https://huagongshe.com/de/reaction/747800

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktSodium CarbonateHCID 10340—
EduktMethanesulfonyl azide, trifluoro-HCID 10986786—
EduktMethyl 3-amino-2-hydroxypropanoate hydrochlorideHCID 71757671—
KatalysatorCopper SulfateHCID 24462—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
ProduktMethyl 3-azido-2-hydroxypropionateHCID 1015411657%

Reaktionsschritte

To an ice-cold mixture of methyl 3-amino-2-hydroxypropionate hydrochloride (19) (27.1 g, 0.17 mol) in water (100 mL) and dichloromethane (100 mL) was added sodium carbonate (19.82 g, 0.187 mol) and CuSO4. 5H2O (0.3 g, 1.2 mmol) with stirring. Triflylazide from experiment 10(B)(i) (crude, 44.6 g, 0.25 mol) was added dropwise keeping the reaction temperature at 0-5° C. Methanol (about 100 mL) was added until the reaction mixture became homogeneous. The reaction mixture was allowed to come to room temperature and then stirred for 20 h. Water (500 mL) was added and the aqueous solution thoroughly extracted with dichloromethane (5×100 mL). The combined organic layers were washed with water (2×200 mL), saturated sodium carbonate (2×200 mL), and then dried (anhydrous sodium sulfate). After removal of the solvent, the residue was chromatographed over silica gel. Elution with 30% ethyl acetate in hexanes furnished the product as a colorless oil (14.0 g; Yield: 57%) Rf 0.57 (30% ethyl acetate in hexanes).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07399460B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-7c25f9a433a94596837ca08a72d607fe
Quellennotizuspto-grants-2008_07