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 400 ml of anhydrous methylene chloride and the mixture was stirred for 15 minutes and was then cooled to -15° C. A solution of 4.3 g of the product of Step G in 10 ml of methylene chloride was added thereto and after 90 minutes, 50 g of celite and 100 ml of ether were added. The mixture was filtered and the filtrate was washed with ether and evaporated to dryness at 30° C. to obtain methyl (5RS) 2-methoxy-5-formyl-1-cyclopentene-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04279919 |
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| Source dataset | uspto-grants-1981_07 |
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| ORD ID | ord-95fcdef23421478ca8f0e145e6ed5adf |
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| Source note | uspto-grants-1981_07 |
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