HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020009Generated: October 29, 2026
Methyl iodide → Ortho-formylphenylacetic acid
https://huagongshe.com/reaction/1020009
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Phthalaldehydic acid | HCID 8406 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ortho-formylphenylacetic acid | HCID 5289058 | 100% |
Reaction Steps
2-Carboxybenzaldehyde (4.53 g, 30 mmoles) was dissolved in acetone (100 mls) and anhydrous potassium carbonate (4.14 g, 30 mmoles) was added. After stirring methyl iodide (5.6 mls, 90 mmoles) was added and the reaction was heated (56° C.) for 30 minutes. The reaction became very thick so further acetone was added (50 mls) and stirring continued at room temperature for a further 72 hours. The reaction mixture was filtered through Celite and then evaporated to leave a viscous oil. The oil was then partitioned between water (30 ml) and ethyl acetate (30 ml). The aqueous layer was washed with further ethyl acetate (2×30 mls) and all the ethyl acetate extracts combined and washed with brine (30 mls) and then water (30 mls) dried over anhydrous magnesium sulphate and evaporated to leave a clear light yellow oil (4.9 g, 100% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716302B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-95265bcc98e24992b2b297b137ee141f |
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| Source note | uspto-grants-2014_05 |
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