Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | p-Toluenesulfonate | HCID 85570 | — |
| Reactant | HCID 86733540 | HCID 86733540 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86733541 | HCID 86733541 | — |
Reaction Steps
p-Toluene sulfonyl chloride (1.425 g., 7.5 mm.) was added at 0°C to a solution of 1.00 g. (5.8 mm.) of isopropyl cis 6-hydroxy-3-hexenoate in 2.37 g. of dry pyridine. The resulting mixture was stirred at 0°C for 4 hours. The crude product was poured on ice and concentrated hydrochloric acid, sodium carbonate till neutral and dried over potassium carbonate. Evaporation of the solvent produced 1.32 g. (70% of theory) of crude tosylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03962354 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-3ce3ea93aefa46e29e39db5cfa09756f |
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| Source note | uspto-grants-1976_06 |
|---|