Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Hydroxyhexadecanoic acid | HCID 92836 | — |
| Solvent | Palmitoyl chloride | HCID 8206 | — |
| Product | 2-Hexadecanoyloxyhexadecanoic acid | HCID 13371862 | — |
Reaction Steps
α-Hydroxypalmiticacid (3.2 g) was dissolved in pridine (15 ml), and palmitoyl chloride (3.3 g) was added thereto under stirring at 0° C. The resulting mixture was allowed to stand over night at room temperature. The reaction mixtue was poured into water and the aqueous solution was stirred at room temperature for 1 hour, followed by acidification with 1 N hydrochloric acid solution, and extraction with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and concentrated to give a residue which was recrystallized from petroleum ether to afford crystals of 2-hexadecanoyloxyhexadecanoic acid (5.4 g). M.p. 55° to 56° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04436726 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-7172565f227e47fa9a3fbb1bf94e9d4b |
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| Source note | uspto-grants-1984_03 |
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