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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1496912Generated: October 26, 2026

Sodium Carbonate → 5-Bromo-2-[4-(trifluoromethoxy)phenyl]pyrimidine

https://huagongshe.com/reaction/1496912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant5-Bromo-2-iodopyrimidineHCID 7006651—
Reactant4-(4-Trifluoromethoxyphenyl)phenolHCID 12008734—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product5-Bromo-2-[4-(trifluoromethoxy)phenyl]pyrimidineHCID 5747928075.2%

Reaction Steps

A mixture of 5-bromo-2-iodopyrimidine (88) (1.50 g, 5.27 mmol), 4-(trifluoromethoxy)phenylboronic acid (44) (1.185 g, 5.75 mmol) and Na2CO3 (1.11 g, 10.5 mmol) in toluene (120 mL) and water (15 mL) was purged with N2. Pd(PPh3)4 (60 mg, 0.05 mmol) was added and the mixture was refluxed under N2 for 17.5 h, then partitioned between EtOAc and water. Column chromatography of the organic portion on silica gel (eluting with 4:1 hexanes/CH2Cl2) gave 5-bromo-2-[4-(trifluoromethoxy)phenyl]pyrimidine (89) (1.264 g, 75%) as a white solid: mp 107-108° C.; 1H NMR (CDCl3) δ 8.83 (s, 2H), 8.46 (d, J=9.0 Hz, 2H), 7.31 (d, J=9.0 Hz, 2H). APCI MS m/z 319, 321 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09198913B2
Source datasetuspto-grants-2015_12
ORD IDord-733afcbff2ad464b97a894ae93ac2805
Source noteuspto-grants-2015_12