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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618702Generated: October 29, 2026

tert-Butyl acrylate → Tert-butyl 4-(1,3-dioxoisoindolin-2-yl)-4-fluoro-4-ethoxycarbonylbutanoate

https://huagongshe.com/reaction/618702

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl acrylateHCID 15458—
ReactantLithium diisopropylamideHCID 2724682—
ReactantEthyl 2-(1,3-dioxoisoindolin-2-yl)-2-fluoroacetateHCID 13594881—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(1,3-dioxoisoindolin-2-yl)-4-fluoro-4-ethoxycarbonylbutanoateHCID 54501069—

Reaction Steps

To a stirred solution of ethyl 2-(1,3-dioxoisoindolin-2-yl)-2-fluoroacetate (0.80 g, 3.2 mmol) in tetrahydrofuran (30 mL) is added lithium diisopropylamide (1.7 mL, 3.4 mmol, 2 M) at -78° C. After 30 minutes, t-butyl acrylate (0.42 g, 3.2 mmol) is added to the mixture which is allowed to reach room temperature. The solvent is removed in vacuo and the residue stirred with methylene chloride (50 mL) and water (30 mL) for 10 min. The organic layer is washed with brine (30 mL), and dried over sodium sulfate. The solvent is removed in vacuo to give tert-butyl 4-(1,3-dioxoisoindolin-2-yl)-4-fluoro-4-ethoxycarbonylbutanoate which is further purified by column chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05955476
Source datasetuspto-grants-1999_09
ORD IDord-9ef903f8855141efa4a361e0e3776543
Source noteuspto-grants-1999_09