Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 16-Hydroxyhexadecanoic acid | HCID 10466 | — |
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18688956 | HCID 18688956 | 64% |
Reaction Steps
16-Hydroxyhexadecanoic acid (6.81 g, 25.0 mmol) was dissolved in tetrahydrofuran (150 ml) and the solution was cooled to 0° C. before adding pyridine (2.73 g, 34.5 mmol). Methacryloyl chloride (2.61 g, 25.0 mmol) was dissolved in tetrahydrofuran (75 ml) and added dropwise. The mixture was stirred for 1 hour at 0° C., and then at room temperature for 24 hours. The solvent was removed under reduced pressure (room temperature), the residue suspended in ether (100 ml) and the mixture washed with distilled water. The ether layer was dried (MgSO4) and the ether evaporated. Chromatographic purification on a silica gel column (1:2 ethyl acetate/hexane) afforded 5.0 g (64%) of the title compound. 1H NMR (60 MHz, CDCl3): δ1.3 (br s, 26H, (CH2)13), 1.95 (m, 3H, C=CCH3), 2.1-2.6 (m, 2H, CH2COO), 4.0-4.4 (m, 2H, COOCH2), 5.52 (m, 1H, vinyl), 6.10 (m, 1H, vinyl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05536490 |
|---|
| Source dataset | uspto-grants-1996_07 |
|---|
| ORD ID | ord-a0b09fcd44ec4ff1a8b64561c03a23e8 |
|---|
| Source note | uspto-grants-1996_07 |
|---|