Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | HCID 15067586 | HCID 15067586 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15067588 | HCID 15067588 | — |
Reaction Steps
An ethereal diazomethane solution is added to a solution of 5 mg of 5-[2-[(1E,3E)-(5RS)-5-hydroxy-1,3-tridecadienyl]-phenyl]-pentanoic acid (produced in example 9) in 0.5 ml of methylene chloride at 0° C. until permanent yellow dyeing and stirred for 5 minutes at 0° C. Then, it is concentrated by evaporation in a vacuum and the residue is chromatographed on silica gel. With hexane/0-80% of ether, 2.6 mg of the title compound is obtained as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05196570 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-10813aadb6f74ba88c7c4f6a7a7f6059 |
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| Source note | uspto-grants-1993_03 |
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