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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 451768Erstellt: 25. Oktober 2026

Ammonium Chloride → (S)-tert-butyl 1-cyclohexyl-3-hydroxypentan-2-ylcarbamate

https://huagongshe.com/reaction/451768

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktSodium borohydrideHCID 4311764—
Edukt(S)-tert-butyl 1-cyclohexyl-3-oxopentan-2-ylcarbamateHCID 15730499—
LösungsmittelMeOH tetrahydrofuranHCID 21899815—
Produkt(S)-tert-butyl 1-cyclohexyl-3-hydroxypentan-2-ylcarbamateHCID 59201568—

Reaktionsschritte

To a solution of (S)-tert-butyl 1-cyclohexyl-3-oxopentan-2-ylcarbamate in THF/MeOH (604/15 mL) at 0° C. was carefully added NaBH4 (630 mg, 16.66 mmol). After 20 min, sat. aq. NH4Cl was added to quench the reaction, and extracted with EtOAc, washed with brine, dried over Na2SO4, filtered, and concentrated to give (S)-tert-butyl 1-cyclohexyl-3-hydroxypentan-2-ylcarbamate (4.77 g, 96%, in a ratio of 40:60) as a white solid. MS ESI +ve m/z 286 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08487108B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-0db4cce6a1e04c7090574e707c3d1e2a
Quellennotizuspto-grants-2013_07