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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2103788Erstellt: 26. Oktober 2026

Benzyl Salicylate → Benzyl 2-[2,6-Bis(isopropyl)phenoxycarbonyloxy]-benzoate

https://huagongshe.com/reaction/2103788

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl SalicylateHCID 8363—
EduktTriethylamineHCID 8471—
Edukt2,6-Di(propan-2-yl)phenyl carbonochloridateHCID 271619—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelCitric AcidHCID 311—
LösungsmittelDichloromethaneHCID 6344—
ProduktBenzyl 2-[2,6-Bis(isopropyl)phenoxycarbonyloxy]-benzoateHCID 2111001757%

Reaktionsschritte

To a cooled (0° C.) solution of benzyl salicylate (0.77 g, 3.3 mmol) in dichloromethane (6 mL) was added triethylamine (0.52 mL, 3.7 mmol) and a catalytic amount of DMAP. To this mixture a suspension of compound (104) (0.9 g, 3.7 mmol, crude product from last step) in dichloromethane (4 mL) was further added. The reaction was allowed to warm to room temperature slowly and stirred for 14 h. The reaction mixture was then diluted with 10% aqueous citric acid solution (10 mL) and extracted with ethyl ether (2×40 mL). The organic phase was dried over MgSO4 and concentrated in vacuo. The residue was purified by radial chromatography on silica gel (eluting with ethyl acetate/hexane) to afford 0.8 g (57% yield over two steps) of the title compound (105).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07576127B2
Quelldatensatzuspto-grants-2009_08
ORD IDord-274f4251ac5f470e866c915c104f7fc3
Quellennotizuspto-grants-2009_08