HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331107Generated: October 25, 2026
Triisopropyl phosphite → Ethyl 3-methylenecyclopentanecarboxylate
https://huagongshe.com/reaction/331107
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triisopropyl phosphite | HCID 8304 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | 2-(Trimethylsilylmethyl)allyl acetate | HCID 4428347 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 3-methylenecyclopentanecarboxylate | HCID 13350809 | 132.6% |
Reaction Steps
The following reaction was performed in a 15 mL sealed tube, behind a safety shield. To 2-((trimethylsilyl)methyl)allyl acetate (2.227 mL, 10.73 mmol) in toluene (2 mL) was sequentially added ethyl acrylate (2.92 mL, 26.8 mmol), triisopropyl phosphite (1.474 mL, 6.44 mmol) and palladium(II)acetate (0.241 g, 1.073 mmol). The contents were purged with nitrogen gas for 5 min. and heated at 100° C. for 45 h. The reaction mixture was cooled to RT and concentrated under reduced pressure. The liquid was transferred to a 50 mL round bottom flask and distilled using a high vacuum pump. Fractions distilling at 50° C. were collected and concentrated to yield 1.317 g (80%) of ethyl 3-methylenecyclopentanecarboxylate. 1H NMR (400 MHz, CDCl3) δ ppm 4.90-4.85 (m, 2H), 4.14 (q, 2H, J=7.0 Hz), 2.87-2.78 (m, 1H), 2.61-2.53 (m, 2H), 2.51-2.23 (m, 2H), 2.09-1.82 (m, 2H), 1.29-1.23 (t, 3H, J=7.2 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877749B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-ab341f62bd45439487fc214d214d21cc |
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| Source note | uspto-grants-2014_11 |
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