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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171885Generated: November 1, 2026

Methyl iodide → Ethyl 1-methylcyclobutanecarboxylate

https://huagongshe.com/reaction/2171885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl cyclobutanecarboxylateHCID 84700—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 1-methylcyclobutanecarboxylateHCID 57538409—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of ethyl cyclobutanecarboxylate (20.0 g, 156.0 mmol) in THF (160 mL) was added dropwise to a cold (−78° C.) solution of LDA (164 mmol of 2M solution) in THF (40 mL). The solution was warmed to 0° C. and then cooled again to −40° C. before the addition of iodomethane (10.2 mL, 163.8 mmol). The solution was slowly warmed to room temperature and stirred overnight. The reaction was quenched with an aqueous saturated solution of ammonium chloride and ether was added. The layers were separated and the aqueous layer was washed with ether. The combined organic layers were washed with 1N HCl then dried over MgSO4. The product was purified by distillation: 1H NMR (400 MHz, MeOD) δ 4.20-4.05 (m, 2H), 2.57-2.33 (m, 2H), 2.08-1.94 (m, 1H), 1.94-1.77 (m, 3H), 1.40 (s, 3H), 1.27 (tt, J=7.1, 1.5 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051319B2
Source datasetuspto-grants-2015_06
ORD IDord-9bc5df15e9a54d3aabec6b20deb5dad1
Source noteuspto-grants-2015_06