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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823886Generated: November 3, 2026

2-Bromo-4'-(trifluoromethyl)acetophenone → HCID 22147881, compound

https://huagongshe.com/reaction/1823886

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4'-(trifluoromethyl)acetophenoneHCID 321979—
Reactant3-Chloro-2-thiophenecarboxamideHCID 2808088—
ProductHCID 22147881HCID 221478816%

Reaction Conditions

Temperature150 °C

Reaction Steps

3-Chloro-thiophene-2-carboxamide (0.145 g, 0.898 mmol) and 4-trifluoromethyl-phenacyl bromide (0.200 g, 0.749 mmol) were placed in a sealed tube and heated at 150° C. for 4 h. The reaction mixture was quenched with ethyl acetate and the residue was purified by column chromatography (gradient 100:1, 20:1 hexane:dichloromethane). The product was further purified by preparative-TLC (100:1, hexane:dichloromethane) to yield 0.0148 g (5.0%) of the title compound as a white solid. 1H NMR (Acetone-d6): 8.58 (s, 1H), 8.01 (d, J=8.1 Hz, 2H), 7.71 (t, 3H), 7.10 (d, J=5.1 Hz, 1H), 7.08 (d, J=5.7 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041685B2
Source datasetuspto-grants-2006_05
ORD IDord-83ba85a6efe34ff0898db704961d6d52
Source noteuspto-grants-2006_05