Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | 12-Hydroxydodecanoic Acid | HCID 79034 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 12-(Acryloyloxy)dodecanoic acid | HCID 22328223 | 40.2% |
Reaction Steps
12-Hydroxydodecanoic acid (5.0 g, 0.023 mol) dissolved in tetrahydrofuran (100 ml) and pyridine (2.16 g, 0.027 mol) was cooled to 0° C. Acryloyl chloride (3.15 g, 0.023 mol) in tetrahydrofuran (75 ml) was then added dropwise to the solution. The mixture was stirred for 5 hours at 0° C. then stirred overnight at room temperature. The precipitated pyridinium salt was filtered off and the solvent removed under vacuum. The resulting liquid was purified by flash chromatography (silica gel/chloroform) to give 2.5 g (40%) of the title compound. 1H NMR (60 MHz, CDCl3): δ 1.20 (s, 18H, CH2), 2.15 (m, 2H, CH2COOH), 4.0 (m, 2H, COOCH2), 5.7-6.0 (m, 3H, CH2 = and =CH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06106806 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-1bded2c7cf87408497e48a59e01bd683 |
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| Source note | uspto-grants-2000_08 |
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