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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609704Generated: October 25, 2026

Phenol → (2,2-Diethoxyethoxy)benzene

https://huagongshe.com/reaction/1609704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantSodium hydrideHCID 24758—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
Product(2,2-Diethoxyethoxy)benzeneHCID 96328—

Reaction Conditions

Temperature110 °C

Reaction Steps

Sodium hydride (5.83 g of a 55% dispersion in mineral oil) was added to a solution of phenol (12.56 g) in DMPU (25 ml) at 5° C. and the mixture was stirred for 30 minutes. Bromoacetaldehyde diethyl acetal (10.05 ml) was added and the mixture was heated at 110° C. for 5 hours, then allowed to cool. The mixture was partitioned between ethyl acetate (100 ml) and water (100 ml) and the organic phase was separated and washed sequentially with aqueous 2M sodium hydroxide solution (2×50 ml) and water (50 ml). The aqueous fractions were combined and re-extracted with ethyl acetate (100 ml). The combined organic extracts were dried (MgSO4) and concentrated. The resultant oil was purified by flash column chromatography, eluting with ethyl acetate/hexane (1:10 v/v) to give 2-phenoxyacetaldehyde diethyl acetal (9.43 g) as an oil; NMR: 1.25(6H,t, J=7.0 Hz), 3.6-3.85(4H,m), 4.05(2 H,d, J=6.0 Hz), 4.85 (1H,t, J=6.0 Hz) and 6.9-7.35(5H,m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401849
Source datasetuspto-grants-1995_03
ORD IDord-c2616766ac3d4775bb739add6494f839
Source noteuspto-grants-1995_03