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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1766140Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1766140

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
PatentnummerUS07230003B2
Quelldatensatzuspto-grants-2007_06
ORD IDord-aa5bbd4bab1142a59edfe362c9369a13
Quellennotizuspto-grants-2007_06