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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432555Generated: October 31, 2026

Methanol → HCID 18759604, compound

https://huagongshe.com/reaction/432555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 18759599HCID 18759599—
Reactant226422-89-5HCID 18759618—
SolventTolueneHCID 1140—
ProductHCID 18759604HCID 18759604—

Reaction Conditions

Temperature100 °C

Reaction Steps

4-(3-Butenyl)phenylboronic acid is made by the method of Nakashima and Irie (Nakashima, H.; Irie, M. Macromol. Chem. Phys. 200, 683-692). 4-(3-butenyl)phenylboronic acid (0.44 g) and a solution of Pd(Ph3)4 (58 mg) in 5 mL of degassed toluene is placed in a 50 mL Schlenk tube. The mixture is purged with nitrogen, after which a solution of 4-bromo-7-phenyl-1,10-phenanthroline (0.670 g) and Na2CO3 (428 mg, 4 mmol) in 5 mL of degassed 4:1H2O/CH3OH is added. The mixture is heated under nitrogen at 100° C. with rapid stirring until TLC monitoring shows the reaction to be complete (ca 24 hrs). The reaction mixture is then added to a separatory funnel and washed with ether (3×50 mL). The combined organic fractions are dried over MgSO4 and concentrated by roto-evaporation. The desired product is purified by column chromatography on silica gel using a mixture of ethyl acetate and hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664111B2
Source datasetuspto-grants-2003_12
ORD IDord-2d581f6149324d8b9d3e18c071d9c5cf
Source noteuspto-grants-2003_12