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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363441Generated: October 30, 2026

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

https://huagongshe.com/reaction/363441

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, 2M) 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 numberUS05874448
Source datasetuspto-grants-1999_02
ORD IDord-ad788feeae5a41e9b9b926821f3e9d1c
Source noteuspto-grants-1999_02