HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276800Generated: October 31, 2026
Methyl iodide → (E)-methyl 4-(dimethoxymethyl)cinnamate
https://huagongshe.com/reaction/276800
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Formylcinnamic acid dimethyl acetal | HCID 86589671 | — |
| Product | (E)-methyl 4-(dimethoxymethyl)cinnamate | HCID 23247180 | 89% |
Reaction Steps
4-Formylcinnamic acid dimethyl acetal (Cleeland, Jr., et al., U.S. Pat. No. 3,969,373) (20.00 g) and anhydrous potassium carbonate (12.44 g) were stirred in anhydrous N,N-dimethylfornamide (189 ml) for 5 minutes. Methyl iodide (12.8 g) was added and the resulting mixture was stirred vigorously with gentle heating (oil bath at 40° C.) for 18 h. Volatiles were evaporated in vacuo and the residue partitioned between hexanes (400 ml) and water (100 ml). The hexanes layer was dried (magnesium sulfate) and evaporated to give (E)-methyl 4-(dimethoxymethyl)cinnamate as a pale yellow oil (18.98 g, 89%), 1H-NMR (DMSO-d6) consistent with structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06355646B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-9ce82db5ae704ec1b35a9d0810a7d640 |
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| Source note | uspto-grants-2002_03 |
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