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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083306Generated: October 31, 2026

Hexane → 1-(2,2-Diethoxyethoxy)-4-fluorobenzene

https://huagongshe.com/reaction/2083306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant4-FluorophenolHCID 9732—
ReactantSodium hydrideHCID 24758—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
SolventDimethylformamideHCID 6228—
Product1-(2,2-Diethoxyethoxy)-4-fluorobenzeneHCID 1144751882%

Reaction Steps

A solution of p-fluorophenol (28.1 g., 0.25 mole) in dimethylformamide (30 ml.) is added dropwise to a suspension of hexane (2 × 30 ml.)-prewashed sodium hydride (50% oil dispersion, 12.5 g., 0.26 mole) in dimethylformamide (120 ml.). The resulting mixture is stirred at room temperature for 10 minutes, treated with bromoacetaldehyde diethylacetal (49.3 g., 0.25 mole), and finally heated on a steam bath for 4 hours. The reaction mixture is allowed to come to room temperature and the precipitated sodium bromide is filtered off. Dimethylformamide is then removed on a rotary evaporator, the oil residue is diluted with acetone (100 ml.) and another quantity of sodium bromide is precipitated which again is removed by filtration. The filtrate is then concentrated on a rotary evaporator leaving an oil residue which is vacuum distilled at 87° C./0.05 mm. to yield the desired product as colorless oil (46.7 g., 0.205 mole, 82%). ir (neat) 3.4~3.5, 6.21, 6.64, 8.00, 8.25, 8.83, 9.32, 12.08, 13.20μ; pmr (CCl4)δ1.17 (6H, t, J=7.5Hz), 3.57 (2H, q, J=7.5Hz), 3.61 (2H, q, J=7.5Hz), 3.85 (2H, d, J=5Hz). 4.68 (1H, t, J=5Hz), 6.6-7.1 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04085125
Source datasetuspto-grants-1978_04
ORD IDord-54aaf908cbb24650b4b91350915cf41c
Source noteuspto-grants-1978_04