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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250792Generated: October 30, 2026

2,2-Dimethoxypropane → HCID 14768058, compound

https://huagongshe.com/reaction/1250792

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-DimethoxypropaneHCID 6495—
ReactantBenzaldehyde, 4-(2-hydroxyethoxy)-HCID 89178—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 14768058HCID 1476805870%

Reaction Steps

To a solution of 4-hydroxyethoxybenzaldehyde (Bernstein et al., J. Am. Chem. Soc., 73: 906-912 (1951); 8.5 g, 51.2 mmol), 2,2-dimethoxypropane (30 mL, 244 mmol) in a mixture of methanol (40 mL) and CH2Cl2 (100 mL) was added anhydrous Amberlyst 15 (Aldrich) (1.0 g). The mixture was stirred for 5 hours, the catalyst was removed by filtration and the filtrate was concentrated to give the crude product contaminated with the starting aldehyde. This material was chromatographed on silica eluting with 1:1 ethyl acetate-hexane. The pure product fractions were pooled and concentrated. Drying under vacuum afforded 7.6 g (70%) of the title compound as a pale yellow, viscous liquid. 1H NMR: d 7.28 (d, J=9 Hz, 2 H), 6.92 (d, J=9 Hz, 2H), 5.31 (s, 1H), 4.86 (t, J=5.5 Hz, 1H), 3.98 (t, J=5 Hz, 2H), 3.71 (q, J=5 Hz, 2H), 3.20 (s, 3H). 13C NMR: d 158.60, 130.19, 127.74, 113.90, 102.46, 69.43, 59.52, 52.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339147B1
Source datasetuspto-grants-2002_01
ORD IDord-1be8c702989649f3b0adce683c4c24a2
Source noteuspto-grants-2002_01