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HRID 82763Erstellt: 24. Oktober 2026

(R)-(+)-N-(tert-Butoxycarbonyl)-O-(tert-butyldimethylsilyl)serinol → HCID 178454221, Verbindung

https://huagongshe.com/de/reaction/82763

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(R)-(+)-N-(tert-Butoxycarbonyl)-O-(tert-butyldimethylsilyl)serinolHCID 10913779—
EduktPotassium tert-butoxideHCID 23665647—
EduktHCID 178441319HCID 178441319—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 178454221HCID 17845422169,8%

Reaktionsschritte

A mixture of Example 32B (87 mg, 0.2 mmol), (R)-tert-butyl 2-{[tert-butyl(dimethyl)silyl]oxy}-1-(hydroxymethyl)ethylcarbamate (62 mg, 0.2 mmol) and 1N potassium tert-butoxide in THF (0.2 mL, 0.2 mmol) in THF (10 mL) was stirred at room temperature for 1 hour. The mixture was concentrated under reduced pressure and the residue was partitioned between EtOAc and water. The organic layer was washed with brine, dried with MgSO4 and concentrated under reduced pressure to afford 100 mg of the title compound. MS (DCI/NH3) m/z 716 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846730B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-092630b413da4ad78796f56ff50981ec
Quellennotizuspto-grants-2014_09