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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18796Generated: October 29, 2026

Trifluoroacetic acid → HCID 59655349, compound

https://huagongshe.com/reaction/18796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
Reactant2-[2-(4-Fluorophenyl)-2-oxoethyl]-cis-4,5-diphenyl-4,5-dihydro-imidazole-1-carboxylic Acid, Tert-Butyl EsterHCID 86596337—
SolventDichloromethaneHCID 6344—
ProductHCID 59655349HCID 5965534947.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold (0° C.) solution of 257 (458 mg, 1.0 mmol) in dichloromethane (25 mL) is added TFA (1.5 mL). The reaction mixture is stirred for 20 min. at 0° C., and at RT for 30 min. The solution is poured into cold sat. sodium bicarbonate solution, and the mixture extracted with EtOAc. The organic layer is separated, dried (MgSO4), and filtered. The filtrate is rotary evaporated, and the residue is recrystallized from Et2O to give 170 mg of the product 258. 1H NMR (CDCl3) δ 10.60-8.80 (bs, 1 H), 8.00-7.80 (m, 2 H), 7.20-7.00 (m, 9 H), 7.00-6.85 (m, 4 H), 5.50 (bs, 1 H), 5.30 (s, 2 H); MS: m/z 359 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741493B2
Source datasetuspto-grants-2010_06
ORD IDord-3bb81985b11e4679b8520068d299f10a
Source noteuspto-grants-2010_06