HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromo-m-cresol → HCID 66643648, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromo-m-cresol | HCID 72857 | — |
| Reactant | HCID 86052179 | HCID 86052179 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66643648 | HCID 66643648 | — |
Reaction Steps
Intermediate 4-(4′-methoxymethoxy-3′-iso-propylbenzyl)-3-methyl-phenol was prepared from 4-bromo-3-methyl-phenol (J. Med. Chem. 12:1350 (1980)) and 4-methoxymethoxy-3-iso-propylbenzaldehyde 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 used for the synthesis of compound 7. 1H NMR (300 MHz, DMSO-d6): δ 9.04 (s, 1H), 7.02-6.99 (d, J=8.7 Hz, 1H), 6.92 (s, 1H), 6.81-6.76 (m, 2H), 6.67 (s, 2H), 4.03 (d, J=10.5 Hz, 2H), 3.76 (s, 2H), 3.16-3.14 (m, 1H), 2.19 (s, 3H), 1.14-1.12 (d, J=6.9 Hz, 6H); TLC conditions: Uniplate silica gel, 250 microns; Mobile phase=ethyl acetate; Rf=0.11;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07514419B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-aef11faffd3d4dc5ab42861eea08197e |
| Source note | uspto-grants-2009_04 |