HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167397Generated: October 30, 2026
(E)-ethyl 3-(4-(benzyloxy)-3,5-difluorophenyl)-2-methylacrylate → HCID 59419852, compound
https://huagongshe.com/reaction/2167397
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (E)-ethyl 3-(4-(benzyloxy)-3,5-difluorophenyl)-2-methylacrylate | HCID 59419841 | — |
| Reactant | HCID 90442472 | HCID 90442472 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | HCID 178418390 | HCID 178418390 | — |
| Product | HCID 59419852 | HCID 59419852 | — |
| Product | HCID 90406564 | HCID 90406564 | — |
Reaction Steps
Into a 100-mL round-bottom flask, was placed a solution of ethyl (2E)-3-[3-(benzyloxy)-2,4-difluorophenyl]-2-methylprop-2-enoate and ethyl (2E)-3-[4-(benzyloxy)-3,5-difluorophenyl]-2-methylprop-2-enoate (4 g, 12.04 mmol, 1.00 equiv) in EtOAc (50 ml) and palladium carbon (2.5 g). Into the resulting mixture was then introduced H2(g). The resulting solution was stirred overnight at 25° C. The solids were filtered out and the resulting mixture was concentrated under vacuum. The resulting residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:4) to yield ethyl 3-(3,5-difluoro-4-hydroxyphenyl)-2-methylpropanoate and ethyl 3-(3-(benzyloxy)-2,4-difluorophenyl)-2-methylpropanoate as colorless 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-18c1680e8cc94f5898d2035f3703607f |
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| Source note | uspto-grants-2015_06 |
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