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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 217907Erstellt: 23. Oktober 2026

tert-Butanol → N-Cbz-4-[(2,3-Dihydroxypropyloxy)phenyl]butylamine

https://huagongshe.com/de/reaction/217907

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-ButanolHCID 6386—
EduktN-Methylmorpholine N-oxide monohydrateHCID 2724197—
Edukt[4-(4-Allyloxyphenyl)butyl]carbamic acid benzyl esterHCID 11551825—
EduktSodium BisulfiteHCID 23665763—
KatalysatorOsmium TetroxideHCID 30318—
LösungsmittelPropan-2-one--water (1/1)HCID 18366337—
ProduktN-Cbz-4-[(2,3-Dihydroxypropyloxy)phenyl]butylamineHCID 1155979462%

Reaktionsschritte

A solution of osmium tetroxide (50 mg, 0.2 mmol) in tert-butanol (8 mL) was added to a solution of 4-methylmorpholine N-oxide monohydrate (1.2 g, 9.1 mmol) in 100 mL (1:1) acetone/water solution and the mixture was stirred for 10 min at room temperature. After this time, 30 (3.1 g, 9.0 mmol) was added in 50 mL (1:1) acetone/water solution. The reaction mixture was stirred at room temperature overnight, then NaHSO3 (0.5 g) was added and the stirring was continued for 15 min. The acetone was evaporated and the pH was adjusted to 5.5 by the addition of 2N HCl then the mixture was extracted with ethyl acetate. The organic fraction was isolated, dried with sodium sulfate, and filtered through silica gel. Compound 31 (2.1 g, 62%) was isolated as a white solid after removing the solvent and drying under vacuum. 1H NMR (300 MHz, DMSO-d6) δ 1.48 (m, 2H), 1.50 (m, 2H), 2.46 (m, 2H), 3.00 (m, 2H), 3.43 (m, 2H), 3.80 (m, 2H), 3.93 (t, 1H), 4.66 (d, 1H), 4.99 (s, 2H), 6.82 (d, 2H), 7.07 (d, 2H), 7.26 (s, 1H), 7.33 (s, 5H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08198286B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-a2127e81f42b41ce9e2c3fc910f2cafe
Quellennotizuspto-grants-2012_06