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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083186Generated: November 1, 2026

Hexane → HCID 86735621, compound

https://huagongshe.com/reaction/2083186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant1,8-OctanedithiolHCID 14493—
Reactant(Chlorothio)formyl chlorideHCID 75990—
ReactantThiocarbonic acid, anhydrosulphide with methyl thiohypochloriteHCID 123417—
ReactantHCID 12418459HCID 12418459—
Solvent1-ButanolHCID 263—
ProductHCID 86735621HCID 8673562198.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-Butoxycarbonylsulfenyl chloride, with a boiling point of 83°-90° C. at 13 mm., was prepared in 84.3% yield by a procedure analogous to that described for methoxycarbonylsulfenyl chloride in Example I by reacting equimolar quantities of 1-butanol and chlorocarbonylsulfenyl chloride. To a stirred solution of 8.4 grams (0.05 mole) of 1-butoxycarbonylsulfenyl chloride and 25 milliliters of hexane was added dropwise with stirring and under nitrogen at 0° C., 4.4 grams (0.025 mole) of 1,8-octanedithiol dissolved in 25 milliliters of hexane. After allowing the solution to warm to room temperature, the solution was concentrated under reduced pressure to give 10.9 grams (98.2%) of 1,8-bis(1-butoxycarbonyldithio)-octane as a pale yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04085094
Source datasetuspto-grants-1978_04
ORD IDord-772e5b3eb3664a67beadea93e1e62a2f
Source noteuspto-grants-1978_04