Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 131717832 | HCID 131717832 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 131717831 | HCID 131717831 | — |
Reaction Steps
For acetylation, 0.5 ml of acetic anhydride is added to a solution of 310 mg of the above-described alcohol in 2 ml of pyridine and stirred for 16 hours at 25° C. Then, it is concentrated by evaporation with adding toluene in a vacuum and the residue is chromatographed on silica gel. With hexane/1-5% of methyl-tert-butyl ether, 265 mg of 5-[(1E,3E)-(5RS)-5-acetoxy-1,3-tridecadienyl]-phenyl]-pentan-1-ol-diphenyl-tert-butylsilyl ether 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-e72e7b95caa44ca09c1ae260594782c8 |
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| Source note | uspto-grants-1993_03 |
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