Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 970327Generated: October 29, 2026

Bromobenzene → 2-Fluoro-5-phenylamino-terephthalic Acid Dimethyl Ester

https://huagongshe.com/reaction/970327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantCesium carbonateHCID 10796—
ReactantDimethyl 2-amino-5-fluoroterephthalateHCID 16748146—
Catalystpalladium(II) acetateHCID 167845—
CatalystBinap, (A+-)-HCID 634876—
SolventTolueneHCID 1140—
Product2-Fluoro-5-phenylamino-terephthalic Acid Dimethyl EsterHCID 1674863880.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a mixture of 174B (10.0 g, 44.0 mmol), bromobenzene (4.6 mL, 44.0 mmol), (S)-(−)-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl (2.06 g, 3.30 mmol), and toluene (250 mL) was added cesium carbonate (20.0 g, 44.0 mmol) followed by palladium(II) acetate (0.494 g, 2.20 mmol). The mixture was heated at 90° C. for 24 h. HPLC indicated that the reaction was complete. The reaction mixture was cooled to room temperature, and filtered under reduced pressure through a pad of Celite topped with a pad of silica gel, and the Celite/Silica gel pad was rinsed with EtOAc. The filtrate was concentrated under reduced pressure and purified by silica gel chromatography using a 1:10 mixture of EtOAc and hexane to give 10.7 g (80%) of compound 174C as a pale yellow solid. HPLC retention time=3.72 min. (Condition A). 1H-NMR (400 MHz, CDCl3) δ 3.89 (s, 3H), 3.93 (s, 3H), 7.12 (m, 1H), 7.22 (m, 2H), 7.37 (m, 2H), 7.74 (m, 2H), and 9.22 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07312209B2
Source datasetuspto-grants-2007_12
ORD IDord-49b6917dfa0d409ba894878291e297dc
Source noteuspto-grants-2007_12