HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526773Generated: November 4, 2026
Potassium Carbonate → HCID 86709940, compound
https://huagongshe.com/reaction/1526773
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Chloromethoxy)-2-methoxyethane | HCID 77590 | — |
| Reactant | 5-bromo-3-tert-butyl-2-hydroxybenzaldehyde | HCID 797006 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86709940 | HCID 86709940 | 106.7% |
Reaction Steps
A mixture of 5-bromo-3-(tert-butyl)-2-hydroxybenzaldehyde (4.74 g, 18.42 mmol) and anhydrous potassium carbonate (2.83 g, 20.45 mmol) in anhydrous DMF (20.0 mL) was stirred under nitrogen in a water bath (20° C.) to give an orange-yellow suspension. After stirring for 20 min, 2-methoxyethoxymethyl chloride (2.40 mL, 21.19 mmol, technical grade) was added drop wise (20 min) to above suspension while maintaining an internal temperature of 20° C. The reaction mixture was stirred at room temperature for 3 h to give a canary yellow suspension. The reaction mixture was poured into ice-water (150 mL) and stirred at room temperature to give a yellow oily liquid, no solid formation was observed. After 30 min of stirring, the reaction mixture was extracted with dichloromethane (2×75 mL). The organic layer was removed, washed with water (1×50 mL) and dried over anhydrous magnesium sulfate, filtered and evaporated in-vacuo to give a pale yellow viscous liquid (6.7832 g). No purification was necessary and the crude product (purity >97%) was used directly in the next Step #3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09085606B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-43a66aeefbcc4257b1ffac18684dea89 |
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| Source note | uspto-grants-2015_07 |
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