Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 1,8-Octanedithiol | HCID 14493 | — |
| Reactant | (Chlorothio)formyl chloride | HCID 75990 | — |
| Reactant | Thiocarbonic acid, anhydrosulphide with methyl thiohypochlorite | HCID 123417 | — |
| Reactant | HCID 12418459 | HCID 12418459 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 86735621 | HCID 86735621 | 98.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04085094 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-772e5b3eb3664a67beadea93e1e62a2f |
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| Source note | uspto-grants-1978_04 |
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