Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutyric Acid | HCID 6590 | — |
| Reactant | HCID 131729082 | HCID 131729082 | — |
| Catalyst | HCID 178418778 | HCID 178418778 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 131729083 | HCID 131729083 | — |
Reaction Steps
2-Methylpropanoic acid (5 mL) and silver (I) oxide (2.3 g) were charged to a vessel at room temperature. 1-Chloro-2-methylpropyl (4-methylthiophenoxy)formate (2.46 g) D4 was added to the reaction vessel. The reaction was heated to 95° C. and the mixture was maintained at approximately 90° C. for 1 hour. The reaction was then cooled to room temperature and tert-butyl methyl ether (20 mL) was added. The solid was filtered and the filter was washed with tert-butyl methyl ether (2×15 mL). The organic phase was washed with water (4×25 mL), bicarbonate (2×25 mL), and dried over sodium sulfate. The organic volatiles were removed under vacuum to provide 3.2 g of the title compound D5 as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989641B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-131c3c6e138d409b8efa76dc9ea51e7f |
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| Source note | uspto-grants-2011_08 |
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