Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | L-Ascorbic Acid | HCID 54670067 | — |
| Reactant | HCID 86672618 | HCID 86672618 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 131731341 | HCID 131731341 | — |
Reaction Steps
0.71 mL (5.1 mmol) of triethylamine was added and dissolved in a suspension of 0.82 g (4.63 mmol) of ascorbic acid in acetonitrile (9 mL). The above crude product of (5,9,13,17-tetramethyloctadec-4-enyl)tosylate was added at room temperature, and the reaction mixture was heated for 2 hours at 90° C. The reaction mixture was concentrated, and the resulting residue was purified by silica gel column chromatography (methanol/methylene chloride mixture) to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703922B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-c595c19e7312427bbddc7658d9808c97 |
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| Source note | uspto-grants-2014_04 |
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