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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337618Generated: October 29, 2026

4-Chloro-3-methylphenol → HCID 22467254, compound

https://huagongshe.com/reaction/337618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-3-methylphenolHCID 1732—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromoethyl methyl etherHCID 80972—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 22467254HCID 22467254—

Reaction Steps

To a stirred solution of 4-chloro-3-methylphenol (1 eq.) in DMF (0.7 M) was added K2CO3 (1.2 eq.). The mixture was stirred at 50° C. for 5 min before 1-bromo-2-methoxyethane (1.5 eq.) was added. After 2 h at 70° C., the reaction mixture was cooled down to RT and then diluted with water and ether. The organic phase was separated and washed sequentially with 2 N aq. NaOH, water and brine. The organic extract was dried over Na2SO4, filtered and the filtrate concentrated in vacuo to afford the title compound as a yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889714B2
Source datasetuspto-grants-2014_11
ORD IDord-ce8696ec85d046e4b4bc07a5a4c1936d
Source noteuspto-grants-2014_11