HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroethanol → Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate) | HCID 6639 | 88.4% |
Reaction Conditions
| Temperature | 2.5 °C |
|---|
Reaction Steps
In a typical run, p-toluenesulfonyl chloride (TsCl, 70.5 g, 0.37 mol) was added slowly to a solution of 2-chloroethanol (38; 25.0 g, 0.31 mol) in pyridine (100 mL) at 0° C. The reaction mixture was stirred at 0-5° C. for 18 h. Ice water (300 mL) was added and the resulting mixture was extracted with ethyl acetate (3×100 mL). The combined organic layers were washed with 1 N HCl (3×100 mL), water (100 mL×3), dried (Na2SO4) and concentrated under reduced pressure to afford 2-chloroethyl 4-methylbenzenesulfonate 39 (64.3 g, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846947B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-8d9e6a3f48bc427483e6475ed283561b |
| Source note | uspto-grants-2014_09 |