Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 13194898 | HCID 13194898 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13194899 | HCID 13194899 | — |
Reaction Steps
25.5 g of chromic oxide were added in small fractions at 15° to 20° C to a solution of 41 ml of pyridine in 400ml of anhydrous methylene chloride and the mixture was stirred for 15 minutes. The mixture was cooled to -15° C and a solution of 4.3 g of the product of Step A in 10 ml of methylene chloride was added thereto. After 11/2 hours, 50 g of celite and 100 ml of ether were added thereto and the mixture was filtered. The filtrate was washed with ether and the filtrate was evaporated to dryness at 30° C to obtain methyl (5RS) 2-methoxy-5-formyl-1-cyclopentenecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04097494 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-3122bd6f3ca8425990b356c914867507 |
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| Source note | uspto-grants-1978_06 |
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