HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519685Generated: November 4, 2026
Trimethyl orthoformate → HCID 86679260, compound
https://huagongshe.com/reaction/1519685
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- | HCID 18462 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86679257 | HCID 86679257 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 86679260 | HCID 86679260 | 67% |
Reaction Steps
Trimethyl orthoformate (51 g) and (+)-CSA (2.3 g) were added to a methanol (0.40 L)-chloroform (0.10 L) mixed solution of ethyl 4-[(4-formylphenyl)ethynyl]benzoate (27 g) as obtained in Example 10-(1), and the mixture was stirred for 3 hours at room temperature. A saturated aqueous solution of sodium hydrogen carbonate was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate, and then the desiccant was filtered out. Then, the solvent was distilled off under reduced pressure, and the resulting residue was purified by OH type silica gel chromatography (gradient elution with hexane/ethyl acetate=95/5→80/20) to obtain ethyl 4-{[4-(dimethoxymethyl)phenyl]ethynyl}benzoate (white solid) (21 g, 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073821B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-3c99620bc79945d1aa7c6b6e017ac72b |
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| Source note | uspto-grants-2015_07 |
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