HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855024Generated: November 1, 2026
Methyl chloroformate → 1-Ethyl 1-methyl 4,4-dimethoxycyclohexane-1,1-dicarboxylate
https://huagongshe.com/reaction/1855024
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl 4,4-dimethoxycyclohexane-1-carboxylate | HCID 13746868 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Ethyl 1-methyl 4,4-dimethoxycyclohexane-1,1-dicarboxylate | HCID 90409912 | 93% |
Reaction Steps
To a −78° C. solution of iPr2NEt (3.95 mL, 27.7 mmol) in THF (50 mL) was added n-BuLi (17.3 mL of a 1.6 M solution in hexanes; 27.7 mmol) was added. After 15 min, ethyl 4,4-dimethoxycyclohexane-carboxylate (4.0 g, 18.50 mmol) was added and the reaction mixture was stirred at −78° C. for 1 h. Methyl chloroformate (2.87 mL, 37.0 mmol) was added and the reaction mixture was warmed to rt. The reaction was quenched with saturated aqueous NH4Cl and extracted with EtOAc (100 mL). The organic layer was dried (Na2SO4) and concentrated in vacuo. The crude oil was chromatographed (SiO2; continuous gradient from 0 to 20% EtOAc:hexanes) to afford the title compound (4.7 g, 93% yield) as a clear oil. 1H NMR (500 MHz, CDCl3) δ 4.21 (q, J=7.1 Hz, 2H), 3.75 (s, 3H), 3.19 (s, 6H), 2.16-2.05 (m, 4H), 1.79-1.69 (m, 4H), 1.27 (t, J=7.1 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962660B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-c51c0c97070d4c2598db687da4866168 |
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| Source note | uspto-grants-2015_02 |
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