Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86619970 | HCID 86619970 | — |
Reaction Steps
In 100 ml of methylene chloride were dissolved 10 g (79 mmol) of oxalyl chloride, to which a solution of 4.4 g (79 mmol) of propargyl alcohol and 6.4 ml (79 mmol) of pyridine dissolved in 30 ml of methylene chloride was slowly added dropwise over 1 hour with cooling with ice. The resulting mixture was stirred for 30 minutes at room temperature to produce propynyl chloroglyoxylate in the reaction system. Subsequently, a solution of 14.5 g (79 mmol) of pentafluorophenol and 6.4 ml (79 mmol) of pyridine dissolved in 30 ml of methylene chloride was slowly added dropwise to the reaction system with cooling with ice. The resulting mixture was stirred for 1 hour at room temperature and then filtered, washed with water, dried over anhydrous magnesium sulfate and concentrated. The thus obtained crude product was purified by crystallization to obtain 2.1 g of 2-propynyl pentafluorophenyl oxalate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07794876B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-bad90afb449b4930b91526d6ead33cfe |
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| Source note | uspto-grants-2010_09 |
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