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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500338Generated: November 1, 2026

Methyl iodide → HCID 14194550, compound

https://huagongshe.com/reaction/1500338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 14040059HCID 14040059—
ReactantEthyl acetate hexaneHCID 21226206—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14194550HCID 1419455092%

Reaction Conditions

Temperature10 °C

Reaction Steps

50 g (1 eq) tert-butyl 3-(tert-butyldimethylsilyloxy)propylcarbamate dissolved in 200 ml THF were added dropwise to a mixture of 20.7 g (5 eq) sodium hydride and 300 ml THF at 0° C. After heating the reaction mixture to 10° C., 32.3 ml (3 eq) methyl iodide were added dropwise. On completion of the addition, the mixture was stirred for 3 h at room temperature. The reaction course was monitored by thin-layer chromatography (30% EtOAc/hexane). Once the conversion was complete, the reaction mixture was quenched with saturated NH4Cl solution and then extracted with ethyl acetate. The combined organic phases were dried over Na2SO4. Following removal of the solvent under reduced pressure, 48 g (92%) of product were obtained in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206156B2
Source datasetuspto-grants-2015_12
ORD IDord-ab3570366c08464e9e91158365634d82
Source noteuspto-grants-2015_12