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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439613Generated: October 27, 2026

Trifluoroacetic acid → HCID 86749475, compound

https://huagongshe.com/reaction/439613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86749476HCID 86749476—
SolventDichloromethaneHCID 6344—
ProductHCID 86749475HCID 8674947581%

Reaction Steps

To a solution of (3E,4E)-1-t-butoxycarbonylmethyl-3-benzylidene-4-(3,4,5-trimethoxybenzylidene)-2,5-pyrrolidinedione (3.5 g) obtained in Example 42 in dichloromethane (40 ml) is added trifluoroacetic acid (10 ml) at room temperature, and the mixture is allowed to stand for 4 hours. The mixture is evaporated under reduced pressure to remove the solvent, and to the residue is added trichloromethane. The mixture is washed, dried, and evaporated to remove the solvent. The resulting residue is crystallized from diethyl ether to give (3E,4E)-1-carboxymethyl-3-benzylidene-4-(3,4,5-trimethoxybenzylidene)-2,5-pyrrolidinedione (2.5 g) as yellow prisms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05514815
Source datasetuspto-grants-1996_05
ORD IDord-2d8eee9ff3304f4db1a716624acab3aa
Source noteuspto-grants-1996_05