Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178470565 | HCID 178470565 | — |
| Product | HCID 20064731 | HCID 20064731 | 42.2% |
Reaction Steps
A reaction vessel was charged with 96.4 g (400 mmol) of ethyl 2-hydroxy-4-trifluoromethyl-5-thiazolecarboxylate and 117 g (766 mmol) of phosphorus oxychloride and then cooled in an ice bath. To the cooled mixture was added 40 g of diethylamine. The reaction mixture was heated at reflux at 163° C. with stirring for about 14 hours. Excess phosphorus oxychloride was removed under reduced pressure. The residue was poured into ice water and a solid precipitate was collected. The solid precipitate was dissolved in ethyl ether, washed with 5% sodium hydroxide, dried with calcium sulfate, and concentrated under reduced pressure to provide 50 g of residue. This residue was subjected to Kugelrohr distillation (100°-120° C. @ 0.5 mm Hg) to provide 3.5 g of a yellow liquid identified in Table I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05000775 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-59ac93a27c3b4c1dbf52494466069f9d |
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| Source note | uspto-grants-1991_03 |
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