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-propylbenzyl)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 G. Chiellini et al. Biorg. Med. Chem. Lett. 2000, 10, 2607 and transformed into the title compound by the procedure described for the synthesis of compound 7: 1H NMR (300 MHz, DMSO-d6): δ6.93 (s, 1 H), 6.75 (d, J=8.4 Hz, 1 H), 6.65 (d, J=8.4 Hz, 1 H), 6.64 (s, 1 H), 4.09 (d, J=9.9 Hz, 2 H), 3.79 (s, 2 H), 3.77 (s, 3 H), 3.34 (m, 1 H), 2.22 (s, 3 H), 2.20 (s, 3 H), 2.10 (s, 3 H), 1.31 (d, J=7.2 Hz, 6 H); LC-MS m/z=391 [C21H29O5P−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07829552B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-138ee03ea6a24ad9b080cc22fff5b169 |
| Source note | uspto-grants-2010_11 |