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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683964Generated: November 4, 2026

Trifluoroacetic acid → HCID 86749475, compound

https://huagongshe.com/reaction/1683964

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 (3 E,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 numberUS05639789
Source datasetuspto-grants-1997_06
ORD IDord-1c0d1692d59a42d59fb7664e835777b0
Source noteuspto-grants-1997_06