HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667774Generated: November 1, 2026
Potassium Carbonate → HCID 67428436, compound
https://huagongshe.com/reaction/1667774
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-(2-Bromoethoxy)tetrahydro-2H-pyran | HCID 86621 | — |
| Reactant | HCID 67426546 | HCID 67426546 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67428436 | HCID 67428436 | 58.7% |
Reaction Steps
A mixture of 0.374 g (2 mmole) of 5-fluoro-2-methoxy-4-nitro-phenol, 0.439 g (2.10 mmole) of 2-(2-bromo-ethoxy)-tetrahydro-pyran, 0.828 g (6.0 mmole) of potassium carbonate and 5 mL of dimethylformamide was heated at 80 degrees for 4 hours. The cooled mixture was poured into 50 mL of dilute ammonium chloride solution and extracted three times with 25 mL of ethyl acetate. The combined organic extracts were washed three times with 25 mL of water, once with 25 mL of brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with ethyl acetate-hexanes (gradient 20:80-30:70) to give 0.370 g of 2-[2-(5-fluoro-2-methoxy-4-nitro-phenoxy)-ethoxy]-tetrahydro-pyran (IV.44) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044213B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-a12e779b4ae7417f9a4f0adfb6261062 |
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| Source note | uspto-grants-2011_10 |
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