Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | p-Toluenesulfonate | HCID 85570 | — |
| Reactant | HCID 15396982 | HCID 15396982 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86733539 | HCID 86733539 | — |
Reaction Steps
p-Toluene sulfonyl chloride (1.425 g., 7.5 mm.) was added at 0°C to a solution of 1.00g. (6.95 mm.) of methyl 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, extracted with benzene, washed with 2N hydrochloric acid, sodium carbonate till neutral and dried over potassium carbonate. Evaporation of the solvent produced 1.425 g. (68% 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-d1c5699f027c4d29bf116e78220a1a5e |
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| Source note | uspto-grants-1976_06 |
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