HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172233Generated: October 31, 2026
Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester → HCID 66852034, compound
https://huagongshe.com/reaction/1172233
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester | HCID 70670 | — |
| Reactant | HCID 58967062 | HCID 58967062 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66852034 | HCID 66852034 | 99.3% |
Reaction Steps
6-(t-Butyldimethylsilanyloxymethyl)pyridine-2-carboxaldehyde (4.29 g) was dissolved in 50 mL of DMF, and 7.14 g of (carbethoxymethylene)triphenylphosphorane was added to the solution, and then the mixture was stirred at room temperature for 1 hour. The reaction mixture was poured into ice-water, and extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate, and concentrated to dryness under reduced pressure. To the residue, 100 mL of a mixture of hexane-ethyl acetate (5:1) was added, the insoluble material was filtrated off, and the filtrate was concentrated under reduced pressure. The residue was purified by chromatography on silica gel (hexane-ethyl acetate=10:1) to give 5.45 g of ethyl 3-[6-(t-butyldimethylsilanyloxymethyl)pyridin-2-yl]acrylate as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834002B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-d4bad23217054c958cc720f6fb8f7a95 |
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| Source note | uspto-grants-2010_11 |
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