Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | L-Ascorbic Acid | HCID 54670067 | — |
| Reactant | HCID 86672628 | HCID 86672628 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 131731342 | HCID 131731342 | — |
Reaction Steps
0.49 mL (3.5 mmol) of triethylamine was added and dissolved in a suspension of 0.56 g (3.2 mmol) of ascorbic acid in acetonitrile (7 mL). After the above crude product of (4,8,12,16-tetramethylheptadec-3-enyl)tosylate was added at room temperature, 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-fc2eb04c09f243eab5f9bfe1c6c678d1 |
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| Source note | uspto-grants-2014_04 |
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