HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → Methyl 4-(3-iodo-4-methoxyphenyl)-3-methylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Methyl 4-(4-methoxyphenyl)-3-methylbenzoate | HCID 67065985 | — |
| Catalyst | Silver sulfate | HCID 159865 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 4-(3-iodo-4-methoxyphenyl)-3-methylbenzoate | HCID 57692978 | — |
Reaction Steps
Into a 10000-mL 4-necked round-bottom flask was placed methyl 4-(4-methoxyphenyl)-3-methylbenzoate (470 g, 1.83 mol, 1.00 equiv), Ag2SO4 (572.8 g, 1.84 mol, 1.00 equiv), iodine (466.3 g, 1.84 mol, 1.00 equiv), methanol (4000 mL), ethyl acetate (1000 mL). The resulting solution was stirred for 3 h at room temperature. The resulting mixture was concentrated under vacuum. The residue was diluted with 3000/1500 mL of EtOAc/brine. The solid was filtered out. The filtrate was extracted with 2×1000 mL of ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 630 g (crude) of methyl 4-(3-iodo-4-methoxyphenyl)-3-methylbenzoate as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09221834B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-2ae7fe74232746579f1de0d8dfaaf2ef |
| Source note | uspto-grants-2015_12 |