HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266637Generated: October 31, 2026
2,2-Dimethoxypropane → HCID 14768058, compound
https://huagongshe.com/reaction/1266637
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2-Dimethoxypropane | HCID 6495 | — |
| Reactant | Benzaldehyde, 4-(2-hydroxyethoxy)- | HCID 89178 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14768058 | HCID 14768058 | 70% |
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 hrs, 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, 2H), 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06548652B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-ce4cfc4b4fca434f9766b1fbd47ba4f4 |
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| Source note | uspto-grants-2003_04 |
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