Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275903Generated: October 23, 2026

4-Methoxy-3-methylbenzyl chloride → HCID 22117274, compound

https://huagongshe.com/en/reaction/1275903

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-3-methylbenzyl chlorideHCID 143742—
ReactantHCID 22117273HCID 22117273—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22117274HCID 22117274—

Reaction Conditions

Temperature0 °C

Reaction Steps

n-Butyllithium (14.4 ml, 2.5M solution in hexane) was added dropwise to a stirred solution of the product from step (i) (6.9 g) in THF (100 ml) at 0° C. The solution was stirred at 0° C. for 1 hour and then transferred by cannula into a solution of 4-chloromethyl-1-methoxy-2-methylbenzene (J. Chem. Soc. 1956, 2455) (5.86 g) in THF (60 ml) at -30° C. The mixture was stirred for 1 hour and allowed to warm to room temperature. After 30 minutes the reaction was quenched with water. The mixture was partitioned between ethyl acetate and water. The organic phase was washed with water, dried (MgSO4) and evaporated. Purification was by chromatography eluting with 5% ethyl acetate in isohexane. Yield 2.16 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06162808
Source datasetuspto-grants-2000_12
ORD IDord-3586f2b78c074b26a38a61144b804e66
Source noteuspto-grants-2000_12