HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 66642817, compound → HCID 66642767, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 66642817 | HCID 66642817 | — |
| Reactant | 2,5-Dimethyl-4-triisopropylsilanyloxy-benzaldehyde | HCID 86052187 | — |
| Product | HCID 66642767 | HCID 66642767 | — |
Reaction Steps
Intermediate 2,5-dimethyl-4-(4′-methoxy-2′-methyl-3′-iso-propyl-benzyl) phenol was prepared from 2,5-dimethyl-4-triisopropylsilanyloxy-benzaldehyde and 1-bromo-4-methoxy-2-methyl-3-iso-propylbenzene according to the procedure described in Chiellini et al., Bioorg. Med. Chem. Lett. 10:2607 (2000) and transformed into the title compound by the procedure described for the synthesis of compound 7: 1H NMR (300 MHz, DMSO-d6): δ 6.93 (s, 1H), 6.75 (d, J=8.4 Hz, 1H), 6.65 (d, J=8.4 Hz, 1H), 6.64 (s, 1H), 4.09 (d, J=9.9 Hz, 2H), 3.79 (s, 2H), 3.77 (s, 3H), 3.34 (m, 1H), 2.22 (s, 3H), 2.20 (s, 3H), 2.10 (s, 3H), 1.31 (d, J=7.2 Hz, 6H); LC-MS m/z=391 [C21H29O5P−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07514419B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-0241f8a8b26f4e54aaec3c8905f29466 |
| Source note | uspto-grants-2009_04 |