HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → HCID 57704787, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Ethylacetate methanol | HCID 21584119 | — |
| Reactant | HCID 67065969 | HCID 67065969 | — |
| Catalyst | HCID 178418844 | HCID 178418844 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57704787 | HCID 57704787 | — |
Reaction Steps
To a mixture of silver sulfate (0.97 g, 3.11 mmol) and iodine (0.79 g, 3.11 mmol) in MeOH (20 ml) at room temperature, a solution of methyl 2-chloro-4′-methoxybiphenyl-4-carboxylate (0.86 g, 3.11 mmol) in 1:1 mixture of MeOH/EtOAc (10 ml) was added. The mixture was stirred at room temperature for 6 h until color of the reaction turned to pale. The solid was filtered off and the filtrate was concentrated. The title compound was obtained after flash column using EtOAc:hexane/5:95 as the eluant. 1H NMR (CDCl3, 500 MHz): δ 8.15 (d, J=1.5 Hz, 1H), 7.97 (dd, J=8, 2Hz, 1H), 7.89 (d, J=2 Hz, 1H), 7.46 (dd, J=8.5, 2 Hz, 1H), 7.40 (d, J=8 Hz, 1H), 6.91 (d, J=8 Hz, 1H), 3.98 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08440702B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-43d71bc3598548949b972e2b55647660 |
| Source note | uspto-grants-2013_05 |