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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426702Generated: October 30, 2026

Ethanethiol → HCID 22808762, compound

https://huagongshe.com/reaction/426702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantSodium hydrideHCID 24758—
ReactantHCID 22808737HCID 22808737—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22808762HCID 22808762—

Reaction Steps

Ethyl mercaptan (0.1 ml) was injected dropwise into a slurry of 1.0 ml THF and 62.5 mg of sodium hydride (50% in oil). The resultant slurry was stirred for 1.0 hour at 25° whereupon a solution of 167 mg 1-Bromo-16,20-methanoprost-13E-en-9-one in 1.0 ml of THF was injected and the reaction mixture was stirred for 3.0 hours at 25°. The reaction mixture was quenched by the addition of 10% aqueous HCl and extracted twice with chloroform. The chloroform extracts were washed with saturated aqueous NaHCO3 and then brine. They were dried (Na2SO4), filtered and evaporated in vacuo to yield 135 mg of an orange oil. The oil was chromatographed (85:15 silicic acid-Celite, benzene-ethyl acetate gradient elution) to afford 70.1 mg of a clear oil having the following structure: ##STR58## The structure of this material was confirmed by nuclear magnetic resonance and mass spectral analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04171331
Source datasetuspto-grants-1979_10
ORD IDord-fa3511a6ce7c4e508d33a5d285252339
Source noteuspto-grants-1979_10