HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597775Generated: October 30, 2026
Water → 2-(Methoxymethoxy)-4-(phenylmethoxy)benzaldehyde
https://huagongshe.com/reaction/597775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Benzyloxy-2-hydroxybenzaldehyde | HCID 561235 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Methoxymethoxy)-4-(phenylmethoxy)benzaldehyde | HCID 17862060 | — |
Reaction Steps
N,N-diisopropylethylamine (1.98 ml) and chloromethyl methyl ether (0.76 ml) were added to a solution of 4-benzyloxy-2-hydroxybenzaldehyde (2071 mg) in tetrahydrofuran (30 ml), and this reaction mixture was stirred and heated under reflux for 19 hours. N,N-diisopropylethylamine (2.7 ml) and chloromethyl methyl ether (1.04 ml) were further added, and the resulting mixture was stirred and heated under reflux for another 10 hours. After water was added, the reaction mixture was extracted with ethyl acetate, washed with a saturated aqueous ammonium chloride solution and saturated brine, dried over anhydrous magnesium sulfate, then filtered through silica gel and alumina. The filtrate was concentrated under reduced pressure to give the title compound (2470 mg). This compound was used in the following reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897387B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-c33085f8c1744614a8e04291c2341459 |
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| Source note | uspto-grants-2011_03 |
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