HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854541Generated: October 29, 2026
Iodine → 3-(4-Iodomethyl-2-methyl-phenyl)-propionic acid methyl ester
https://huagongshe.com/reaction/854541
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-(4-Hydroxymethyl-2-methyl-phenyl)-propionic Acid Methyl Ester | HCID 57431976 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Sodium Bisulfite | HCID 23665763 | — |
| Product | 3-(4-Iodomethyl-2-methyl-phenyl)-propionic acid methyl ester | HCID 57431974 | — |
Reaction Steps
A mixture of 3-(4-Hydroxymethyl-2-methyl-phenyl)-propionic acid methyl ester (0.62 g, 2.98 mmol), triphenyl phosphine (0.86 g, 3.27 mmol) and dichloromethane (10 mL) is stirred at room temperature. A solution of iodine (0.83 g, 3.27 mmol) in benzene (5 mL) is added and the black mixture is stirred at room temperature 2 hr. The brown mixture is diluted with 10% aqueous sodium hydrogen sulfite (5 mL) and the resulting clear mixture is washed with ethyl acetate (3×50 mL). The combined extracts are dried over anhydrous magnesium sulfate, filtered and concentrated. The residue is purified via silica chromatography eluting with 9:1 hexanes:ethyl acetate to afford the title compound as a crystalline ivory solid, 0.68 g, 72%. MS M++1 319. The structure is confirmed by 1H NMR spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07259175B2 |
|---|
| Source dataset | uspto-grants-2007_08 |
|---|
| ORD ID | ord-64fffc6354914cc680d0f9c4f75ce5b5 |
|---|
| Source note | uspto-grants-2007_08 |
|---|