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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363548Generated: October 30, 2026

2,4-Hexadien-1-OL → 4,4'-Di-2,4-hexadienoxybenzophenone

https://huagongshe.com/reaction/363548

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Hexadien-1-OLHCID 8104—
Reactant4,4'-DifluorobenzophenoneHCID 9582—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product4,4'-Di-2,4-hexadienoxybenzophenoneHCID 5387537050.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

4,4'-Difluorobenzophenone (34) (4.8 grams, 22 mmol) was dissolved in anhydrous DMF (1 liter). NaH (95%; 5.6 grams, 220 mmol) was added and the solution was cooled to 0° C. 2,4-Hexadienol (5.8 mL, 51 mmol) was slowly added to the solution and the reaction mixture was allowed to warm to room temperature with stirring under argon overnight. The reaction mixture was concentrated in vacuo, dissolved in dichloromethane, and washed with water. The organic phase was dried (MgSO4) and concentrated and purified by column chromatography (silica gel; hexane/CH2Cl2, 1/3) to afford 2.07 grams (25%) of compound 35 as a white solid. 1H H NMR (300 MHz, DMSO-d6) δ1.73 (d, J=6.6 Hz, 6H), 4.68 (d, J=6.0 Hz, 4H), 5.69-5.84 (m, 4H), 6.05-6.19 (m, 2H), 6.31-6.45 (m, 2H), 7.08 (d, J=9.0 Hz, 4H), 7.68 (d, J=10.2 Hz, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05874532
Source datasetuspto-grants-1999_02
ORD IDord-ad308aeb976141c2818013435a3597f8
Source noteuspto-grants-1999_02