Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526754Generated: October 29, 2026

Phenol → HCID 25248372, compound

https://huagongshe.com/reaction/526754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantSodium hydrideHCID 24758—
Reactant1,2-Difluoro-4-nitrobenzeneHCID 123053—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 25248372HCID 2524837244%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

Sodium hydride (1.51 g, 62.92 mmol, 2.00 equiv) was added in small portions to a solution of phenol (3.25 g, 34.53 mmol, 1.10 equiv) in N,N-dimethylformamide (50 mL) maintained under nitrogen at 0-5° C. After stirring for 30 min at 0-5° C., 1,2-difluoro-4-nitrobenzene (5 g, 31.43 mmol, 1.00 equiv) was added. The reaction mixture was stirred overnight at room temperature and then diluted with 200 mL of water. The resulting solution was extracted with 3×100 mL of ethyl acetate. The combined organic layers was washed with 3×150 mL of brine, dried over anhydrous sodium sulfate and concentrated. The residue was purified on a silica gel column eluted with 0-2% ethyl acetate in petroleum ether to afford 3.2 g (44%) of 2-fluoro-4-nitro-1-phenoxybenzene as a yellow solid. 1H-NMR (400 MHz, CDCl3): δ 8.10-8.07 (m, 1H), 7.99-7.94 (m, 1H), 7.46-7.41 (m, 2H), 7.30-7.26 (m, 1H), 7.12-7.04 (m, 2H), 7.02-6.93 (m, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346761B2
Source datasetuspto-grants-2016_05
ORD IDord-0385dc25b0964613a329bfc4a3d088fd
Source noteuspto-grants-2016_05