HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558434Generated: October 25, 2026
Trimethyl orthoformate → Ethyl 3-dimethoxymethyl-4-methoxybenzoate
https://huagongshe.com/reaction/558434
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | Ethyl 3-formyl-4-methoxybenzoate | HCID 638670 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl 3-dimethoxymethyl-4-methoxybenzoate | HCID 23141411 | 97% |
Reaction Steps
Ethyl 3-formyl-4-methoxybenzoate (500 mg) obtained in step C of Example 1-2-1 was dissolved in 10 mL of methanol. Trimethyl orthoformate (263 μL) and 41 mg of p-toluenesulfonic acid monohydrate were added to the solution, and then the mixture was heated for 2 hours under reflux. After the reaction solution was cooled, 5 mL of a saturated aqueous solution of sodium bicarbonate was added, and the resulting mixture was concentrated under reduced pressure. The residue was diluted with ethyl acetate, washed with purified water and then with a saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate. The anhydrous sodium sulfate was separated by filtration, whereafter the filtrate was concentrated under reduced pressure. The residue was dried under reduced pressure to obtain 596 mg (97%) of ethyl 3-dimethoxymethyl-4-methoxybenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063046B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-48dbf8b5698148bba2bc54c8f0b52c3a |
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| Source note | uspto-grants-2011_11 |
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