HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383134Generated: October 30, 2026
Imidazole → 4-Iodomethyl-2-(2-methylphenyl)benzoic acid, methyl ester
https://huagongshe.com/reaction/383134
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-Hydroxymethyl-2-(2-methylphenyl)benzoic acid methyl ester | HCID 11391208 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Diethylether hexane | HCID 21584099 | — |
| Product | 4-Iodomethyl-2-(2-methylphenyl)benzoic acid, methyl ester | HCID 20699916 | 71.5% |
Reaction Steps
Triphenylphosphine (5.16 g), and imidazole (1.34 g) were dissolved in 3:1 ether:acetonitrile (80 mL), and the reaction was cooled to 0° C. Iodine (5.0 g) was added with vigorous stirring, and the reaction was warmed to ambient temperature. After 1 h, the reaction was recooled to 0° C. and 4-hydroxymethyl-2-(2-methylphenyl)benzoic acid, methyl ester (example 1178C, 4.6 g) was added as a solution in ether (20 mL). After 4 h at ambient temperature, the reaction was diluted with hexane/ether (1:1, 200 mL) and filtered. The filtrate was washed with a dilute solution of Na2SO3 until colorless, then with water (2×50 mL). The organic extracts were washed with brine (20 mL), dried (MgSO4), filtered and concentrated. The residue was purified by silica gel chromatography eluting with 10% EtOAc/hexane to give a light yellow oil (4.7 g) which slowly crystalizes in the freezer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310095B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-7c95752e82e0463b9b91e422b2c52f22 |
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| Source note | uspto-grants-2001_10 |
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