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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19193Erstellt: 24. Oktober 2026

Hydrochloric Acid → (R)-4-Hydroxymethyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester

https://huagongshe.com/de/reaction/19193

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktWaterHCID 962—
Edukt3-Boc-2,2-dimethyloxazolidine-4-carboxaldehyde, (S)-(-)-HCID 179824—
EduktSodium borohydrideHCID 4311764—
LösungsmittelIsopropanolHCID 3776—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(R)-4-Hydroxymethyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl esterHCID 1105346493,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To an ice cold mixture of (S)-4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid t-butyl ester (2.00 g, 8.72 mmol) in tetrahydrofuran (15 mL) and isopropanol (15 mL) was added sodium borohydride (0.99 g, 26.17 mmol). After addition was complete the mixture was stirred at 0° C. for 1 h. Upon completion of the reaction 1N aqueous hydrochloric acid (10 mL) was slowly added. The mixture was poured into water and extracted with ethyl acetate (3×30 mL). The combined organic fractions were washed with a saturated sodium chloride solution and dried over magnesium sulfate. The crude product obtained (R)-4-hydroxymethyl-2,2-dimethyl-oxazolidine-3-carboxylic acid t-butyl ester (1.88 g, 93%) as a colorless oil and was used without further purification: LR-ES-MS m/z calculated for C11H21NO4 [M]+ 231, observed 232 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741327B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-a2b07bf43b7a4a938fb6c9aa3aad7dce
Quellennotizuspto-grants-2010_06