Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | 1-Octanethiol | HCID 8144 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Product | HCID 23707025 | HCID 23707025 | 96% |
Reaction Steps
438.9 g (520.6 ml, 3 moles) of 1-octanethiol were refluxed (with stirring) for about 1 hour with 66 g. (1 mole 85% purity) potassium hydroxide flakes. 72.5 ml (91.33 g., 1.2 moles) of CS2 were then added (dropwise) with stirring to the mixture which had been cooled to 0° C. in an ice-water bath. The mixture was stirred for about 1 hour after addition was complete, and then allowed to warm to room temperature. The resulting white solid precipitate was filtered, thoroughly washed with anhydrous ethyl ether, and dried overnight in a vacuum oven at 35° C. 250.1 g. of potassium octylthioxanthate were obtained (96% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05034141 |
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| Source dataset | uspto-grants-1991_07 |
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| ORD ID | ord-7ebbea74e2984f348d797a15f2f9ad79 |
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| Source note | uspto-grants-1991_07 |
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