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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766140Generated: October 26, 2026

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

https://huagongshe.com/reaction/1766140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl SalicylateHCID 8363—
ReactantTriethylamineHCID 8471—
Reactant2,6-Di(propan-2-yl)phenyl carbonochloridateHCID 271619—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventCitric AcidHCID 311—
SolventDichloromethaneHCID 6344—
ProductBenzyl 2-[2,6-Bis(isopropyl)phenoxycarbonyloxy]-benzoateHCID 2111001757%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230003B2
Source datasetuspto-grants-2007_06
ORD IDord-aa5bbd4bab1142a59edfe362c9369a13
Source noteuspto-grants-2007_06