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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076048Generated: November 2, 2026

Hydrogen Sulfide → HCID 54565844, compound

https://huagongshe.com/reaction/1076048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
Reactant2-Octenoic acid ethyl esterHCID 23832—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductHCID 54565844HCID 54565844—

Reaction Steps

0.2 g of sodium are dissolved in 10 ml of absolute ethyl alcohol. After completed alcoholate-formation, 5 g of 2-octenoic acid ethyl ester are added and the solution is cooled to -70°. At this temperature, 10 ml of hydrogen sulphide are condensed into the solution. Subsequently, the whole mixture is immediately transferred into an autoclave, pre-cooled to about -30°, and left by itself overnight at room temperature in the sealed pressure vessel. On the next morning, the autoclave is heated at 50° for a further 2 hours. After cooling to room temperature, the excess hydrogen sulphide is vented off, the reaction product washed with saturated common salt solution, dried and distilled. There are obtained 1.6 g of 3-mercapto-octanoic acid ethyl ester of boiling point 74°/0.4 mm Hg, nD20 1.4538.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954843
Source datasetuspto-grants-1976_05
ORD IDord-4127d53e387548a3afeb44448a25c778
Source noteuspto-grants-1976_05