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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410059Generated: October 28, 2026

Hydrochloric Acid → HCID 58381689, compound

https://huagongshe.com/reaction/410059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 9855516HCID 9855516—
ReactantHCID 58381726HCID 58381726—
SolventEthanolHCID 702—
ProductHCID 58381689HCID 5838168970%

Reaction Steps

NaOEt (21 wt. % in EtOH, 0.37 mL, 0.98 mmol) was added dropwise to a solution of 2-mercapto-2-ethyl butyric acid (0.08 g, 0.49 mmol) in dry EtOH (7 mL) held at 0° C. under inert atmosphere. The resulting mixture was stirred at 0° C. for 30 minutes before a solution of (5Z,8Z,11Z,14Z,17Z)-icosa-5,8,11,14,17-pentaenyl methanesulfonate (0.15 g, 0.41 mmol) in dry EtOH (3 mL) was added dropwise. The resulting turbid mixture was stirred at ambient temperature for 24 hours, poured into NH4Cl (sat.)(aq.) (15 mL), added 3M HCl to pH ˜2 before extracted twice with EtOAc (2×20 mL). The combined organic extracts were washed with brine (10 mL), dried (MgSO4), filtrated and evaporated in vacuo. The residue was purified by flash chromatography on silica gel using a gradient of 10-25% ethyl acetate in heptane as eluent. Concentration of the appropriate fractions afforded 0.12 g (70% yield) of the title compound as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759558B2
Source datasetuspto-grants-2014_06
ORD IDord-5edae83ee9d545568a29c0565f363ba9
Source noteuspto-grants-2014_06