HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402000Generated: October 28, 2026
Cyclohexyl bromide → 3-Bromo-4-cyclohexyloxy-benzaldehyde
https://huagongshe.com/reaction/402000
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclohexyl bromide | HCID 7960 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromo-4-hydroxybenzaldehyde | HCID 76308 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Bromo-4-cyclohexyloxy-benzaldehyde | HCID 63052639 | 38.4% |
Reaction Steps
3-Bromo-4-hydroxy-benzaldehyde (24.8 mmol, 5.0 g), bromo-cyclohexane (37.3 mmol, 6.08 g) and K2CO3 (37.3 mmol, 5.15 g) were suspended in DMF (15 mL) and stirred over night at 90° C. The mixture was cooled to room temperature, and bromo-cyclohexane (36.8 mmol, 6.0 g) and K2CO3 (36.2 mmol, 5.0 g) were added stirred at 90° C. for another 24 h. The mixture was cooled and filtered. The filtrate was extracted with ethyl acetate. The organic layer was washed with 1.0 N NaOH (200 mL), water, and brine, dried (Na2SO4), filtered, and concentrated under reduced pressure to provide 3-bromo-4-cyclohexyloxy-benzaldehyde (2.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741900B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-c693c0edef2840129bbc2139c0b0b34c |
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| Source note | uspto-grants-2014_06 |
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