HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 68315186, compound → HCID 67207079, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 68315186 | HCID 68315186 | — |
| Reactant | HCID 68315188 | HCID 68315188 | — |
| Reactant | HCID 86671523 | HCID 86671523 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | HCID 67207079 | HCID 67207079 | — |
Reaction Steps
The title compound was prepared by the general procedure described for compound 11a (HU-911), using pinacol arylboronate 4 (mixed with 2) 0.244 g, enol triflate 9a 0.2 g (0.61 mmol), Pd(PPh3)4 0.042 g (0.037 mmol) and t-BuNF 0.91 ml (0.91 mmol, 1M solution in THF) to give colorless oil 170 mg (72%). 1H NMR (300 MHz, CDCl3) δ ppm 6.33 (s, 2H), 6.26 (d, J=3.42 Hz, 1H), 3.71 (s, 6H), 3.47 (s, 3H), 2.55 (t, J=7.70 Hz, 2H), 2.38-2.46 (m, 2H), 1.81-2.03 (m, 2H), 1.56-1.66 (m, 2H), 1.30-1.35 (m, 4H), 1.12 (s, 3H, syn), 1.07-1.16 (m, 1H), 0.97 (s, 3H, anti), 0.90 (t, J=6.84 Hz, 3H). Exact mass calculated for C24H34O4 by the general procedure described for compo4O4: C, 74.58; H, 8.87. Found: C, 74.61; H, 9.04.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365534B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-e7259cf2e5364460b60fa69f5dff678f |
| Source note | uspto-grants-2016_06 |