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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624315Generated: October 30, 2026

Nitrogen → HCID 89724208, compound

https://huagongshe.com/reaction/624315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantWaterHCID 962—
ReactantAcetonitrileHCID 6342—
Reactant1-Ethynyl-4-fluorobenzeneHCID 522627—
ReactantHCID 89724126HCID 89724126—
Catalystpalladium(II) acetateHCID 167845—
SolventEthyl AcetateHCID 8857—
ProductHCID 89724208HCID 8972420874.1%

Reaction Conditions

Temperature75 °C

Reaction Steps

Acetonitrile (31.5 L; 12.5 vol wrt Int-2) in to the reactor under nitrogen atmosphere at ambient temperature. Charged chlorofluoroiodomethoxybenzene (2.5 kg.) into the reactor with stirring. Charged DM water (12.5 L; 5-5.5 Vol wrt Int-2). Charged TEA (1.6 kg; 1.8 eq wrt Int-2) Purged N2 for NLT 60 min. Charged Oxydiphos (0.24 kg; 5 mol % wrt Int-2), Charged Palladium acetate (49 g; 2.5 mol % wrt Int-2), Charged 4-Fluoro phenylacetylene (1.58 kg; 1.5 eq wrt Int-2) with continuous purging of nitrogen1. Continued N2 Purging for NLT 10 min. Raised the temperature to 70-80° C. Stirred the reaction at 70-80° C. for 5 hrs. Reaction progress was monitored by HPLC. Work Up: After completion of the reaction, cooled the reaction mass to 25-30° C. Charged Ethylacetate (7.75 L; 3-3.5 Vol wrt Int-02), stirred for 5 min. Added DM water (4 L; 1.5-1.6 vol wrt Int-02), stirred for 5 min. Removed and retained bottom aqueous phase for further extraction. Remove and retained top organic phase for further wash. Extract the retained aqueous phase with EtOAc (13.4 L, 5-5.5 Vol wrt Int-02). Combined all organic phases and washed with water (8 L; 3-3.5 Vol). Concentrated the organic phases2 on rotovap at 45° C. completely. Purification: Dissolved crude product in MTBE (25 L; 10-1.5 Vol wrt Int-02) at 45 C. Cooled the mass to ambient temperature. Unloaded the reaction mass, rinse the reactor with MTBE (2.5 L; 1.0-1.5 Vol wrt Int-2). Filtered through celite bed, rinse the container with MTBE (2.5 L; 1.0-1.5 Vol wrt Int-2) and filter the rinse. Washed filter bed with MTBE (5.0 L, 2.0-2.5 Vol wrt Int-2). Concentrated under vacuum at 40° C. to 2-3 Vol stage (wrt Int-2). Charged Methanol (17.53 L; 7.0-7.5 Vol wrt Int-02). Concentrate to 2-3 vol stage3 (wrt Int-2). Cooled to 0° C. Filtered the solid. Washed solid with chilled methanol (0° C.) (12.5 L; 5-5.5 Vol wrt Int-02). Suck dried for 1 hr, and then dried in VTD for 5 hr. at 50-55° C. Wt: 1800 g (74.1% yield). Description (color and appearance): Brown crystalline solid. Purity by HPLC (%): 99%; HPLC RT Time 5.656 min under following conditions: Detector: 210 nm; Injection volume 5.00 μL; Run Time 15 min; Column: YMC UltraHT Pro C18 (50 mm×3.0 mm), 2.0μ; Mobile Phase A—0.05% TFA in MillQ Water; Mobile Phase B—0.05% TFA in Acetonitrile; Flow: 1.0 mL/min; Column Oven—40° C.; Time (min)—0 05 10 12 15; B Conc.—10 90 90 10 10. NMR: (1H NMR, 400 MHz, dmso-d6) δ 7.57 (m, 3H), 7.29 (t, 8.8 Hz, 2H), 7.00 (d, 9.2 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303020B2
Source datasetuspto-grants-2016_04
ORD IDord-2d31b249420a4d09bc27ae183095f9e1
Source noteuspto-grants-2016_04