Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 5-Hexyn-1-ol | HCID 70234 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11097066 | HCID 11097066 | — |
Reaction Steps
5-hexyn-1-ol (14 g), pyridine (20 ml) and dichloromethane (60 ml) were mixed and cooled to 0° C. Tosyl chloride (30 g:1.1 equivalent) was added portion wise over 20 minutes. After 5 hours at 0° C., the reaction was transferred to a separating funnel and washed with 2N HCl (2×50 ml) and saturated sodium bicarbonate (2×50 ml). These were back extracted with dichloromethane (1×25 ml) and the combined organic layers washed with water (1×50 ml). After drying (Na2SO4), the liquid was filtered off and the solvent evaporated to leave the product--33.4 g (93%)--of sufficient purity to be used for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05663042 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-4f0435e422b348f4ae60943d2d59d9c0 |
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| Source note | uspto-grants-1997_09 |
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