HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → 4-Phenoxy-2-butyl tosylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Phenoxy-2-butanol | HCID 11378703 | — |
| Product | 4-Phenoxy-2-butyl tosylate | HCID 13326762 | 98% |
Reaction Steps
10 g of the 4-phenoxy-2-butanol was reacted with 13.9 g of p-toluenesulfonyl chloride in 21.2 ml of 5N-sodium hydroxide in accordance with the method described in Norris, J. Am. Chem. Soc. 38, 642 (1907) to obtain 18.9 g of 4-phenoxy-2-butyl tosylate having a boiling point of 170° C. to 171° C. at 2 mmHg in a yield of 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04549023 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-23b6d685725845f1bc1736c6f01b70e1 |
| Source note | uspto-grants-1985_10 |