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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 4,4-dimethoxycyclohexane-1-carboxylateHCID 13746868—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-Ethyl 1-methyl 4,4-dimethoxycyclohexane-1,1-dicarboxylateHCID 9040991293%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962660B2
Source datasetuspto-grants-2015_02
ORD IDord-c51c0c97070d4c2598db687da4866168
Source noteuspto-grants-2015_02