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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300657Generated: October 30, 2026

Triethylamine → HCID 69835843, compound

https://huagongshe.com/reaction/2300657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(4-(Trifluoromethyl)phenyl)butane-1,3-dioneHCID 16640910—
ReactantHCID 18343042HCID 18343042—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventTrimethyl orthoformateHCID 9005—
ProductHCID 69835843HCID 69835843—

Reaction Steps

The title compound was prepared (as described above for the preparation of Example 2) from 176 mg (0.46 mmol) of Intermediate 63, 105 mg (0.46 mmol) of Intermediate 24, and 0.14 mL triethylamine in MeOH (3.0 mL) and trimethylorthoformate (0.75 mL) to yield 152 mg (56% yield) of Example 76 after silica gel chromatography (5%-15% MeOH in DCM): TLC (DCM/MeOH, 4/1): Rf=0.55; 1H NMR (DMSO-d6, 300 MHz) δ11.55 (d, 1H, J=9.0), 7.99-7.94 (m, 4H), 7.73 (d, 2H, J=8.4), 7.33 (t, 2H, J=8.7), 7.16 (d, 2H), J=8.4), 6.90 (d, 2H, J=8.7), 5.61 (s, 1H), 4.93 (s, 2H), 4.23-4.18 (m, 1H), 3.22-3.18 (m, 1H), 2.85-2.73 (m, 4H), 1.72 (s, 3H), 1.17 (t, 3H, J=7.5); low resolution MS (ES+)m/e 597.09 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498174B1
Source datasetuspto-grants-2002_12
ORD IDord-77b77ecbda424de8bd801030a0c6fa61
Source noteuspto-grants-2002_12