Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 86739817 | HCID 86739817 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86739816 | HCID 86739816 | 105.7% |
Reaction Steps
A mixture of 3.3 g of the product of Step B, 30 ml of toluene and 0.33 g of p-toluene sulfonic acid monohydrate was refluxed until gas evolution ceased and was cooled to 20° C. and diluted with ether. The ether phase was washed with water, dried and evaporated to dryness at 40° C. under reduced pressure to obtain 2.9 g of (1R,cis) 2,2-dimethyl-3(Z)-[2-bromo-3-oxo-3-methoxy-propenyl]-cyclopropane-1-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04489093 |
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| Source dataset | uspto-grants-1984_12 |
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| ORD ID | ord-983bff420b414f38b7195f38ac657cba |
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| Source note | uspto-grants-1984_12 |
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