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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226264Generated: October 26, 2026

4-Benzyloxybenzyl chloride → HCID 57754436, compound

https://huagongshe.com/reaction/226264

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyloxybenzyl chlorideHCID 70042—
ReactantLithium diisopropylamideHCID 2724682—
Reactant6,7-Difluoro-2-methylquinolineHCID 22241377—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57754436HCID 57754436—

Reaction Conditions

Temperature-10 °C

Reaction Steps

A solution of 8.9 g (49.6 mmol) of the product from Example 1, step 3 in 90 ml THF is cooled at −50° C. 28.6 ml (57.2 mmol) of a 2M solution of lithium diisopropylamide are added and the solution is allowed to heat to −10° C. After 15′ stirring at this temperature the deep colored solution is again cooled to −50° C. A solution of 11.6 g (49.8 mmol) of 1-benzyloxy-4-chloromethyl-benzene in 60 ml THF is dropped into the cooled solution. The system is allowed to heat to room temperature and stirred overnight. The solvent is evaporated and the residue that solidifies on cooling is stirred with ethyl ether and filtered. The residue is filtered through SiO2 eluting with dichloromethane. The yield is 3.75 g (20%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557212B2
Source datasetuspto-grants-2009_07
ORD IDord-ca395e8fb5b7438997f54e1087e83bcd
Source noteuspto-grants-2009_07