Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255917Generated: November 2, 2026

Phthalimide → HCID 13958749, compound

https://huagongshe.com/reaction/255917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(E)-2-methyl-3-fluoroallyl alcoholHCID 13958748—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13958749HCID 1395874969%

Reaction Steps

A solution of (E)-2-methyl-3-fluoroallyl alcohol (prepared in Step D) (17.11 g), triphenylphosphine (49.80 g), diethyl azodicarboxylate (33.06 g) and phthalimide (27.93 g) in THF (500 ml) is stirred at room temperature overnight. The THF is evaporated and the oily residue is extracted three times with hexane giving a powdery solid which is subsequently extracted three times with ether. The combined extracts are evaporated and the residue (63 g) is purified by chromatography on silica gel (950 g) using a mixture of 20% diethyl ether/light petroleum. The major fraction is a colorless crystalline mass (28.6 g, 69% yield) which is essentially pure product. A small portion can be crystallized from hexane to give (E)-1-phthalimido-2-methyl-3-fluoro-2-propene as colorless plates: m.p. 57°-58° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04699928
Source datasetuspto-grants-1987_10
ORD IDord-a638013f18094c6283913f9e9562083b
Source noteuspto-grants-1987_10