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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072103Generated: October 30, 2026

Trifluoroacetic acid → 5-(3'-Methylaminomethylbiphenyl-4-ylmethyl)thiazolidine-2,4-dione

https://huagongshe.com/reaction/1072103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl [4'-(2,4-dioxothiazolidin-5-ylmethyl)biphenyl-3-ylmethyl]methylcarbamateHCID 10202718—
SolventDichloromethaneHCID 6344—
Product5-(3'-Methylaminomethylbiphenyl-4-ylmethyl)thiazolidine-2,4-dioneHCID 12085486105%

Reaction Steps

18 g (42 mmol) of tert-butyl [4′-(2,4-dioxothiazolidin-5-ylmethyl)biphenyl-3-ylmethyl]methylcarbamate in 250 ml of dichloromethane are introduced into a round-bottomed flask and under a nitrogen stream, and 16 ml (208 mmol) of trifluoroacetic acid are added. The mixture is stirred at room temperature overnight and the reaction medium is hydrolysed with a saturated potassium carbonate solution. The mixture is extracted with dichloromethane, the organic phase decanted off, washed with water, dried over magnesium sulphate and evaporated off. The residue obtained is triturated in ethyl acetate and 14.4 g (78%) of the expected product are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908939B2
Source datasetuspto-grants-2005_06
ORD IDord-a09986d6dca2498ab2dd44f2eec2cf04
Source noteuspto-grants-2005_06