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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410051Generated: October 28, 2026

Sodium hydride → HCID 58381721, compound

https://huagongshe.com/reaction/410051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 2-bromopropionateHCID 79040—
ReactantHCID 58381715HCID 58381715—
SolventDimethylformamideHCID 6228—
SolventHeptaneHCID 8900—
ProductHCID 58381721HCID 5838172192.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

(5Z,8Z,11Z,14Z,17Z)-Icosa-5,8,11,14,17-pentaene-1-thiol (305 mg, 1.00 mmol) was added to a solution of NaH (60% in mineral oil, 44 mg, 1.10 mmol) in dry DMF (10 mL) held at 0° C. under inert atmosphere. After ten minutes ethyl bromopropionate (136 μL, 1.05 mmol) was added and the mixture was stirred for 1.5 hour at 0° C. The reaction mixture was added sat. aq. NH4Cl (20 mL) and heptane (50 mL). The phases were separated and the water phase extracted with heptane (2×25 mL). The combined organics were washed with brine (25 mL), dried (MgSO4), filtered and evaporated to give 376 mg of title compound as crude oil. Purification by flash chromatography on silica gel using gradient elution (starting pure heptane and increasing stepwise to heptane:EtOAc 95:5) afforded 318 mg (79% yield) of the title compound as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759558B2
Source datasetuspto-grants-2014_06
ORD IDord-707a7309ac49489dbbb254cc653ff371
Source noteuspto-grants-2014_06