HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789090Generated: October 31, 2026
HCID 131715222, compound → HCID 131715223, compound
https://huagongshe.com/reaction/1789090
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 131715222 | HCID 131715222 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131715223 | HCID 131715223 | — |
Reaction Steps
To a solution of ethyl 4-[4-[(1,1-dimethylethyl)silyl]oxy-1,7-dioxaspiro[5.5]undec-2-yl]-2-methyl-2E-butenoate, (10.0 g; 27.0 mmoles) in methylene chloride (160 ml) is added finely powdered pyridinium chlorochromate (PCC; 8.7 g; 40.5 mmoles) in a single portion with stirring under nitrogen at 25°. After twenty minutes the reaction mixture is diluted with ether (800 ml) and filtered through celite. The chromium salt residue is washed several times with ether, the washes filtered through celite, and the combined filtrates reduced in volume to 100 ml, filtered through silica gel and concentrated in vacuo to an oil. Chromatography (7.5% ethyl acetate/hexane yields the title compound, 4-[4-[(1,1-dimethylethyl)silyl]oxy-1,7-dioxaspiro[5.5]undec-2-yl]-2-methyl-2E-butenealdehyde; (5.42 g; 54.5%0 as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04686297 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-97558f66ea4445e291a3e8e538aec74a |
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| Source note | uspto-grants-1987_08 |
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