HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748007Generated: October 27, 2026
Dimethylformamide → 3-[2-(4-Fluorophenyl)oxazol-4-ylmethoxy]cyclohexanol
https://huagongshe.com/reaction/748007
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1,3-Cyclohexanediol | HCID 10433 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(Chloromethyl)-2-(4-fluorophenyl)-1,3-oxazole | HCID 16038260 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[2-(4-Fluorophenyl)oxazol-4-ylmethoxy]cyclohexanol | HCID 21980291 | — |
Reaction Steps
With ice-cooling, initially 2.25 g of an 80 percent suspension of sodium hydride and then 5.8 g of 1,3-cyclohexanediol were added to a mixture of 50 ml of dimethylformamide and 50 ml of tetrahydrofuran. The mixture was stirred at about 25° C. for 3 hours. 10.5 g of 4-chloromethyl-2-(4-fluorophenyl)oxazole (1) was then added, the mixture was heated at 70° C. and the reaction was monitored by thin-layer chromatography. After the reaction ended, the mixture was poured into ice-water and extracted with ethyl acetate. The organic phase was separated off, dried and concentrated and the residue was purified on silica gel by flash chromatography (ethyl acetate/n-heptane=1:1). This gave the alcohol 3 as an oil. C16H18FNO3 (291.33) MS(ESI): 292 (M+H+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07399777B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-770e3b4bf0854c4982335188246b756a |
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| Source note | uspto-grants-2008_07 |
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