HuagongsheHuagongshe Chemistry Print Report · For research reference only
o-Iodoanisole → Methyl 3,5-dibromo-4-(3-iodo-4-methoxyphenylthio)phenylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | o-Iodoanisole | HCID 68257 | — |
| Reactant | 2-Isopropylanisole | HCID 270623 | — |
| Reactant | Methyl 3,5-dibromo-4-mercaptophenylacetate | HCID 19101399 | — |
| Product | Methyl 3,5-dibromo-4-(3-iodo-4-methoxyphenylthio)phenylacetate | HCID 19101415 | 83.2% |
Reaction Steps
Following the procedures of Example 1, but substituting 2-iodoanisole for 2-isopropylanisole, methyl 3,5-dibromo-4-mercaptophenylacetate (1 g) was reacted with 2-iodoanisole (0.7 g) to yield the thioether, methyl 3,5-dibromo-4-(3-iodo-4-methoxyphenylthio)phenylacetate (1.4 g) which in turn was oxidized to methyl 3,5-dibromo-4-(3-iodo-4-methoxyphenylsulfonyl)phenylacetate, MP: 127°-129° C. The acetate was saponified to the acid, 3,5-dibromo-4-(3-iodo-4-methoxyphenylsulfonyl)phenylacetic acid, MP: 158°-162° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05284971 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-26ec20d2137d47b8a8041176bf5a81d9 |
| Source note | uspto-grants-1994_02 |