Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Vinylpyridine | HCID 7521 | — |
| Reactant | HCID 178418634 | HCID 178418634 | — |
| Product | HCID 86660912 | HCID 86660912 | 76.7% |
Reaction Steps
Into a 100-mL four-necked flask equipped with a nitrogen gas introduction tube, thermometer, Dimroth condenser, and dropping funnel was introduced 15.22 g (0.20 mol) of thioacetic acid (manufactured by Tokyo Kasei Kogyo Co., Ltd.). The contents began to be stirred, and nitrogen was introduced. Thereafter, the contents were cooled to 5° C. or lower with an ice bath, and 21.03 g (0.20 mol) of 2-vinylpyridine was added dropwise thereto through the dropping funnel over 1 hour. After completion of the dropwise addition, the ice bath was removed, and the mixture was stirred at room temperature for further 1 hour and reacted. After completion of the reaction, the liquid reaction mixture was subjected to vacuum distillation under the conditions of a bath temperature of 120° C. and a pressure of 0.8 kPa to obtain 27.8 g of 2-pyridylethyl thioacetate. As a result of analysis by gas chromatography, the 2-pyridylethyl thioacetate was found to have a purity of 96.8% and the yield thereof was found to be 78.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445731B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-51572c5f6e6646c2b35c28a36fc16f6b |
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| Source note | uspto-grants-2013_05 |
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