HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432667Generated: October 26, 2026
Homophthalic acid → 3-(4-Methoxybenzyl)isocoumarin
https://huagongshe.com/reaction/432667
Participants
| Role | Name | HCID | Charge |
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| Reactant | Homophthalic acid | HCID 66643 | — |
| Reactant | 4-Methoxyphenylacetyl chloride | HCID 2734688 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(4-Methoxybenzyl)isocoumarin | HCID 18760247 | 26% |
Reaction Steps
A well-stirred mixture of homophthalic acid (10 g; 56 mmol) and 2-(4-methoxyphenyl)acetyl chloride (10 g, 230 mmol) was heated at 200° C. for 3 hours under nitrogen then cooled to 50° C. and dissolved in toluene (100 ml), The solvent was removed in vacuo and the residue was dissolved in methanol (100 ml). Silica (30 g) was added and the solvent was removed in vacuo. The crude product, thereby adsorbed onto silica, was applied to the top of a column of silica and purified by chromatography using 10-50% mixtures of ethyl acetate and hexane as eluant. Appropriate fractions were combined and the solvents removed in vacuo to give 3-(4-methoxybenzyl)isocoumarin (0.9 g, 26%) as an oil; δH 3.75 (3H, s), 3.80 (2H, s), 6.50 (1H, s), 6.95 (2H, d, J=8.9 Hz), 7.30 (2H, d, J=8.9 Hz), 7.40-7.90 (3H, m), 8.10 (1H, d); m/z (M+H)+. 267.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06664269B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-63120e174dd04a94ac4274466862b099 |
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| Source note | uspto-grants-2003_12 |
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