HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629132Generated: October 25, 2026
4-Hydroxybenzaldehyde → 4-(3,3-Dimethylbutoxy)benzaldehyde
https://huagongshe.com/reaction/629132
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-Chloro-3,3-dimethylbutane | HCID 76111 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3,3-Dimethylbutoxy)benzaldehyde | HCID 10242087 | 78% |
Reaction Steps
A suspension of 4-hydroxybenzaldehyde (200 mg, 1.64 mmol), 1-chloro-3,3-dimethylbutane (395 mg, 1.97 mmol), sodium iodide (24 mg, 0.16 mmol), and cesium carbonate (800 mg, 2.46 mmol) in anhydrous dimethylformamide (5 mL) was stirred at 80° C. overnight. After cooling to room temperature, solids were filtered and washed with ether. The filtrate was washed with 2 N sodium hydroxide (2×20 mL), water (20 mL), and brine (20 mL), dried over magnesium sulfate, filtered, and concentrated to give 4-(3,3-dimethylbutoxyl)benzaldehyde (262 mg, 78% crude) as a pale yellow oil that was used without further purification or characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315495B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-23997737ec954abd986e8cd86c56a09a |
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| Source note | uspto-grants-2016_04 |
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