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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15718Generated: October 25, 2026

Ethyl chloroformate → Ethyl 1,4-dimethoxy-3-methyl-2-naphthoate

https://huagongshe.com/reaction/15718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant2-Bromo-1,4-dimethoxy-3-methylnaphthaleneHCID 292240—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 1,4-dimethoxy-3-methyl-2-naphthoateHCID 1136935289%

Reaction Conditions

Temperature0 °C

Reaction Steps

n-Butyl lithium (1.6M in hexanes, 4.1 ml, 6.56 mmol) was added dropwise to 2-bromo-1,4-dimethoxy-3-methylnaphthalene (1.537 g, 5.47 mmol) in tetrahydrofuran (30 ml) at −50° C. The reaction was stirred for 30 min at −50° C. before dropwise addition of ethyl chloroformate (1 ml, 10.46 mmol). The reaction was allowed to warm to 0° C. over 18 h quenched by addition of hydrochloric acid (2N) and extracted with ethyl acetate. The extract was dried (Na2SO4) and the solvent evaporated under vacuum. The residue was purified by SPE (silica, 10 g) eluting with 10% ethyl acetate in cyclohexane to give ethyl 1,4-dimethoxy-2-methylnaphthalene-3-carboxylate (1.33 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732622B2
Source datasetuspto-grants-2010_06
ORD IDord-68ac42a1003a457896b8b3eb493ce566
Source noteuspto-grants-2010_06