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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1386667Erstellt: 25. Oktober 2026

Benzyl Bromide → Benzyl (s)-hexahydromandelate

https://huagongshe.com/reaction/1386667

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium HydroxideHCID 14797—
Edukt(2s)-Cyclohexyl(hydroxy)acetic acidHCID 819912—
KatalysatorTetrabutylammonium IodideHCID 67553—
LösungsmittelChloroformHCID 6212—
ProduktBenzyl (s)-hexahydromandelateHCID 5432250577,5%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

A solution of 500 mg (3.2 mmol) of (S)-hexahydromandelic acid and 238 mg (0.6 mmol) of tetrabutylammonium iodide in 6.5 mL of CHCl3 was treated with 6.5 mL of 0.5 N KOH and 0.38 mL (3.2 mmol)of benzyl bromide then stirred at 70° C. for 1.5 h. The reaction was cooled to rt and the layers were separated. The aqueous phase was extracted with 2×50 mL CH2Cl2. The organic phases were combined, dried over Na2SO4 and concentrated. Flash chromatography using 17:3 v/v hexanes/EtOAc as the eluant afforded 616 mg (77%) of the title compound: RF: 0.37 (4:1 v/v hexanes/EtOAc); 1H NMR (300 MHz) δ 1.11-1.38 (m, 11H), 2.65 (d, J=6.3 Hz, 1H), 4.06 (dd, J=6.3, 3.5 Hz, 1H), 5.22 (s, 2H), 7.30-7.39 (m, 5H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06265434B1
Quelldatensatzuspto-grants-2001_07
ORD IDord-69b560becb814bccb0784c184fa67963
Quellennotizuspto-grants-2001_07