HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Amino-2-methoxyphenol → HCID 12016873, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Amino-2-methoxyphenol | HCID 74314 | — |
| Reactant | HCID 12016869 | HCID 12016869 | — |
| Product | HCID 12016873 | HCID 12016873 | — |
Reaction Steps
1-Bromo-2,3,4-trifluoro-5-[(3-hydroxy-4-methoxyphenyl)amino-sulfonyl]benzene and 1-Bromo-4,5,6-trifluoro-2-[(3-hydroxy-4-methoxyphenyl)amino-sulfonyl]benzne were prepared in a manner similar to that described above, beginning with a mixture of 5-bromo-2,3,4-trifluorophenylsulfonyl chloride (Example B) and2-bromo-3,4,5-trifluorophenylsulfonyl chloride (Example C) and 3-hydroxy4-methoxyaniline. The two isomeric compounds were separated by column chromatography (silica gel; ethyl acetate:hexanes, 1:4). 1H-NMR (CDCl3): δ 7.79 (1H, m), 6.72-6.62 (4H, m), 5.65 (1H, s), 3.85 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06417176B2 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-5bfb49cdb25940ad82b851e1883fbc44 |
| Source note | uspto-grants-2002_07 |