Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 2-Thiopheneethanol | HCID 79400 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-Thiopheneethanol tosylate | HCID 3682034 | — |
Reaction Steps
4-toluenesulfonyl chloride (162 g), toluene (363.3 g) and 2-(2-Thienyl)ethanol (104 g) are combined. Triethylamine (93 g) is added maintaining the temperature lower than 45° C. After 4 hrs, the mixture is washed with aqueous phosphoric acid, aqueous sodium hydroxide and then water. The organic phase is distilled off under vacuum. Isopropanol (314 g) and heptanes (365.9 g) are added. The batch is crystallized by cooling and isolated at −15° C. The crystals are filtered and washed with heptanes (175 mL). The crystals are then dried under vacuum at room temperature until a melting point of 30° C. is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08981121B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-d39a6ae4bfcc44b1b338adc147ac8848 |
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| Source note | uspto-grants-2015_03 |
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