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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410056Generated: October 28, 2026

Sodium hydride → HCID 58381710, compound

https://huagongshe.com/reaction/410056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactantethyl 2-bromo-2-methylbutanoateHCID 220969—
ReactantHCID 58381715HCID 58381715—
SolventDimethylformamideHCID 6228—
ProductHCID 58381710HCID 5838171090%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (5Z,8Z,11Z,14Z,17Z)-icosa-5,8,11,14,17-pentaene-1-thiol (305 mg, 1.00 mmol) in dry DMF (10 mL) at 0° C. under inert atmosphere was added NaH (60% in mineral oil, 44 mg, 1.1 mmol). After fifteen minutes ethyl 2-bromo-2-methylbutyrate (154 μL, 1.05 mmol) was added and the mixture was stirred for 1.5 hour at 0° C. The reaction mixture was quenched by addition of sat. aq. NH4Cl (20 mL). Water (20 mL) and heptane (50 mL) were added and the phases were separated. The water phase was extracted with heptane (2×25 mL). The combined organics were washed with water (25 mL) and brine (2×25 mL), dried (MgSO4), filtered and evaporated to give 377 mg of the title compound as a crude oil. Purification by flash chromatography on silica gel using isocratic elution (heptane:EtOAc 98:2) afforded 307 mg (77% yield) of the title compound as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759558B2
Source datasetuspto-grants-2014_06
ORD IDord-0b0d95d87e664f7f92802796bddeb11d
Source noteuspto-grants-2014_06