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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507677Generated: October 26, 2026

Triisopropyl phosphite → Ethyl 3-methylenecyclopentanecarboxylate

https://huagongshe.com/reaction/1507677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl phosphiteHCID 8304—
ReactantEthyl AcrylateHCID 8821—
Reactant2-(Trimethylsilylmethyl)allyl acetateHCID 4428347—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductEthyl 3-methylenecyclopentanecarboxylateHCID 13350809132.6%

Reaction Conditions

Temperature100 °C

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, 2 H), 4.14 (q, 2 H, J=7.0 Hz), 2.87-2.78 (m, 1 H), 2.61-2.53 (m, 2 H), 2.51-2.23 (m, 2 H), 2.09-1.82 (m, 2 H), 1.29-1.23 (t, 3 H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221819B2
Source datasetuspto-grants-2015_12
ORD IDord-df0acd41991d4285bb4731790b985848
Source noteuspto-grants-2015_12