HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541346Generated: October 31, 2026
Dimethyl Carbonate → 4-Cyclobutyl-2-ethyl-5-(methoxycarbonyl)benzoic acid
https://huagongshe.com/reaction/541346
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Carbonate | HCID 12021 | — |
| Reactant | 4-Cyclobutyl-2-ethyl-5-iodobenzoic acid | HCID 68288909 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Cyclobutyl-2-ethyl-5-(methoxycarbonyl)benzoic acid | HCID 68288933 | 69% |
Reaction Steps
To a solution of 4-cyclobutyl-2-ethyl-5-iodobenzoic acid (compound 215.3, 3.30 g, 10.0 mmol, 1.00 equiv) in THF (40 mL) was added n-BuLi (2.5 M, 9.50 mL, 2.38 equiv) dropwise at −78° C. under nitrogen atmosphere. The resulting solution was stirred for another 20 min at the same temperature, followed by the addition of a solution of dimethyl carbonate (2.70 g, 30.0 mmol, 3.00 equiv) in tetrahydrofuran (2 mL) dropwise. The reaction temperature was slowly raised to 25° C. and stirred for another 1 h, then slowly quenched with 50 mL of water. The pH was adjusted to ˜4 with HCl (aq., 1 M) and the resulting mixture was extracted with 100 mL of ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by silica gel chromatography with ethyl acetate/petroleum ether (1:3) as eluent to furnish 1.80 g (69%) of the desired product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871790B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-ca11862a47934f618e979e7dca5691f4 |
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| Source note | uspto-grants-2014_10 |
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