HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395094Generated: October 30, 2026
Ethyl orthoformate → HCID 18972492, compound
https://huagongshe.com/reaction/2395094
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 18972613 | HCID 18972613 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18972492 | HCID 18972492 | — |
Reaction Steps
A solution of 24.15 g of 3,6-dimethoxy-9,9-dimethylxanthene-4-carboxaldehyde in 50 ml of absolute ethanol was treated with 50 ml of triethyl orthoformate. After the addition of 100 mg of p-toluenesulphonic acid monohydrate the mixture was boiled under reflux for 1 hour, then cooled and poured into ice-cold sodium bicarbonate solution, whereupon the mixture was extracted twice with 200 ml of ether each time. The combined extracts were washed neutral with water, dried over Na2SO4 and concentrated. The residue was purified on silica gel with hexane/ethyl acetate, whereby there were obtained 19.6 g of 3,6-dimethoxy-9,9-dimethylxanthene-4-carboxaldehyde dimethyl acetal as a pale yellow oil which crystallized slowly; m.p. 60°-62°, IR 2972, 1606, 1572, 1490 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05811389 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-64fccd2e72e24b86b76dadefc3aef429 |
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| Source note | uspto-grants-1998_09 |
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