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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643282Generated: November 1, 2026

Methyl iodide → (S)-2-((R)-2-(4-Fluoro-3-methylphenyl)-2-methoxyethyl)pent-4-enoic acid

https://huagongshe.com/reaction/1643282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant(S)-2-((R)-2-(4-Fluoro-3-methylphenyl)-2-hydroxyethyl)pent-4-enoic acidHCID 59568774—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-((R)-2-(4-Fluoro-3-methylphenyl)-2-methoxyethyl)pent-4-enoic acidHCID 59568837—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a suspension of 217 mg NaH in 20 mL THF was added (S)-2-((R)-2-(4-fluoro-3-methylphenyl)-2-hydroxyethyl)pent-4-enoic acid in 5 mL THF slowly at room temperature. To this mixture was added methyl iodide (289 μL) dropwise followed by stirring for 3 h at 25° C. The reaction was quenched by the addition of 10 mL 1M HCl and then extracted with ethylacetate (3×30 mL). The combined organic layers were washed with brine (2×20 mL) and dried over sodium sulfate. Evaporation of solvent afforded an oil which was used without further purification in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119692B2
Source datasetuspto-grants-2012_02
ORD IDord-9d82caf123ad422a898567ab32e2940e
Source noteuspto-grants-2012_02