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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158543Generated: November 3, 2026

Water → (4,5-Difluoro-1,2-phenylene)dimethanol

https://huagongshe.com/reaction/1158543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant4,5-Difluorophthalic AnhydrideHCID 639745—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(4,5-Difluoro-1,2-phenylene)dimethanolHCID 1663948285.1%

Reaction Steps

To a solution of LiAlH4 (1M in tetrahydrofuran) (11 ml, 11.0 mmol, 2.0 molar equivalents) cooled to −78° C. was added dropwise a solution of 4,5-difluorophtalic anhydrid (1.0 g, 5.4 mmol, 1 molar equivalent) in THF (5 ml). The reaction mixture was allowed to warm up to room temperature and then stirred at 70° C. for 2 hours. To this resulting solution cooled to 0° C. was added a 2M sodium hydroxide solution (5 ml) followed by cold water (5 ml) and THF (10 ml). The reaction mixture was then further extracted with THF (3 times 20 ml). The organic fractions were combined, washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuum to give a light yellow solid. Purification by recrystallisation from acetone/hexane gave the title compound as light yellow needles (0.8 g, 85%). 1H NMR (300.13 MHz, DMSO) δ(ppm) 4.47 (d, J=5.30, 4H) 5.26 (t, J=5.30 Hz, 2H) 7.36 (t, J=10.10 Hz, 2H). 19F NMR (282.38 MHz, DMSO) δ(ppm) −142.27 (s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807993B2
Source datasetuspto-grants-2010_10
ORD IDord-d787df811b634f4f953063f336019088
Source noteuspto-grants-2010_10