HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375139Generated: October 25, 2026
Ethyl chloroformate → Ethyl 1,4-dimethoxy-3-methyl-2-naphthoate
https://huagongshe.com/reaction/1375139
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 2-Bromo-1,4-dimethoxy-3-methylnaphthalene | HCID 292240 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 1,4-dimethoxy-3-methyl-2-naphthoate | HCID 11369352 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07166631B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-58c8d308fd31452db0c1522c0c54ce8d |
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| Source note | uspto-grants-2007_01 |
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