HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475521Generated: October 29, 2026
Dimethylformamide → HCID 86658986, compound
https://huagongshe.com/reaction/475521
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Methylcyclohexanemethanol | HCID 118193 | — |
| Reactant | 4-Fluoro-3-(trifluoromethyl)benzaldehyde | HCID 522269 | — |
| Product | HCID 86658986 | HCID 86658986 | 87% |
Reaction Steps
30 ml of dried dimethylformamide containing 4-methyl-1-cyclohexanemethanol (1 g, 7.8 mmol) was added to sodium hydride (342.2 mg, 8.58 mmol, 60% dispersed oil) and slowly stirred at room temperature under nitrogen. The mixture was further stirred at room temperature for 30 minutes and added to 5 ml of dried dimethylformamide containing 4-fluoro-3-(trifluoromethyl)benzaldehyde (1.2 g, 7.8 mmol) over 10 minutes. Then, the reaction mixture was stirred at room temperature for 18 hours until the initial product disappeared. 20 ml of ice water was added thereto, and the resulting mixture was extracted with ethyl acetate and water. The organic layer was washed with water several times, dried with anhydrous magnesium sulfate, filtered and solvent-evaporated. The residual oil was chromatographed on the silica gel column (hexane:ethyl acetate=20:1) to afford 4-((methylcyclohexyl)methoxy)-3-(trifluoromethyl)benzaldehyde (1.64 g, yield: 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637558B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-62369728412e462e9ea3bc71b4a15b9d |
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| Source note | uspto-grants-2014_01 |
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