HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → Methyl 2-hydroxy-5-iodo-3-methylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Benzoic acid, 2-hydroxy-3-methyl-, methyl ester | HCID 31835 | — |
| Catalyst | HCID 178418844 | HCID 178418844 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 2-hydroxy-5-iodo-3-methylbenzoate | HCID 14172484 | — |
Reaction Steps
Methyl 2-hydroxy-3-methylbenzoate (0.869 g, 5.23 mmol) in MeOH (5 mL) was added dropwise to a suspension of iodine (1.327 g, 5.23 mmol) and silver sulfate (1.63 g, 5.23 mmol), at room temperature under N2. The resultant brown suspension was stirred for 3 h after which time a colorless suspension was observed. The mixture was filtered through a plug of Celite, washed with MeOH (30 mL) and concentrated in vacuo to afford methyl 2-hydroxy-5-iodo-3-methylbenzoate, as a colorless solid. LCMS calc.=292.1; found=292.7 (M+H)+. 1H NMR (500 MHz, CHCl3): δ 11.0 (s, 1 H); 8.02 (s, 1 H); 7.62 (s, 1 H); 3.97 (s, 3 H); 2.25 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08354454B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-ec589faa79af48cbb226388831828a29 |
| Source note | uspto-grants-2013_01 |