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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066829Generated: October 31, 2026

Toluene → Methyl 4-(5-cyano-7-isopropenyl-1,3-benzoxazol-2-yl)benzoate

https://huagongshe.com/reaction/2066829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 74788214HCID 74788214—
ReactantHCID 86643502HCID 86643502—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductMethyl 4-(5-cyano-7-isopropenyl-1,3-benzoxazol-2-yl)benzoateHCID 68409145—

Reaction Conditions

Temperature91 °C

Reaction Steps

To a 5-l, 3-neck round-bottom flask fitted with a stirring paddle, a condenser blanketed with nitrogen, and a thermocouple, was added 4-(7-bromo-5-cyano-1,3-benzoxazol-2-yl)benzoate (55.5 g, INTERMEDIATE 35), toluene (2 l), water (375 ml), ethanol (150 ml), 2M aqueous sodium carbonate (250 ml), and isoprenylboronic acid (83.4 g, INTERMEDIATE 37). The mixture was purged with nitrogen three times and then tetrakis(triphenylphosphine)palladium(0) (9.1 g) was added, and the mixture was purged three times with nitrogen. The mixture was heated to reflux (91° C.) and stirred at this temperature overnight. The mixture was then cooled to 20° C. and the product was filtered, washed with water, dried, and transferred to a 3-l round-bottom flask and rinsed with toluene (1 l). Residual solvent was removed in vacuo. Mass spectrum (ESI) 319.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293721B2
Source datasetuspto-grants-2012_10
ORD IDord-5ed79b36660d488d9baa241091216cb2
Source noteuspto-grants-2012_10