HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167396Generated: October 30, 2026
Ethyl 2-(triphenylphosphoranylidene)propionate → (E)-ethyl 3-(4-(benzyloxy)-3,5-difluorophenyl)-2-methylacrylate
https://huagongshe.com/reaction/2167396
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-(triphenylphosphoranylidene)propionate | HCID 79792 | — |
| Reactant | 4-(Benzyloxy)-3,5-difluorobenzaldehyde | HCID 15714026 | — |
| Reactant | 2,4-Difluoro-3-(phenylmethoxy)benzaldehyde | HCID 74891943 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (E)-ethyl 3-(4-(benzyloxy)-3,5-difluorophenyl)-2-methylacrylate | HCID 59419841 | — |
| Product | HCID 90442472 | HCID 90442472 | — |
Reaction Steps
Into a 100-mL round-bottom flask, was placed 4-(benzyloxy)-3,5-difluorobenzaldehyde and 3-(benzyloxy)-2,4-difluorobenzaldehyde (4 g, 16.11 mmol, 1.00 equiv, crude), ethyl 2-(triphenylphosphoranylidene)propanoate (8.75 g, 24.14 mmol, 1.50 equiv) and toluene (60 mL). The resulting solution was stirred for 12 h at 110° C. The resulting mixture was then concentrated under vacuum. The resulting residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:8) to yield ethyl (2E)-3-[4-(benzyloxy)-3,5-difluorophenyl]-2-methylprop-2-enoate and ethyl (2E)-3-[3-(benzyloxy)-2,4-difluorophenyl]-2-methylprop-2-enoate as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045454B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-e507a5c0b4f04a3d8047bdb2af9d2268 |
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| Source note | uspto-grants-2015_06 |
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