HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379512Generated: October 31, 2026
Water → 5-Azido-5-(2-methoxyphenyl)-1-pentene
https://huagongshe.com/reaction/379512
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 1-(2-Methoxyphenyl)pent-4-en-1-ol | HCID 15884721 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-Azido-5-(2-methoxyphenyl)-1-pentene | HCID 15884722 | — |
Reaction Steps
To a solution of crude 5-hydroxyl-5-(2-methoxyphenyl)-1-pentene, prepared as described above, in toluene (150 mL) at 0° to 40° C. was added diphenylphosphoryl azide (25.86 mL, 120 mmol) followed by DBU (17.95 mL, 120 mmol) and the resulting reaction mixture was stirred at room temperature (20° C. to 25° C.) for 28 hours. H2O was added, the aqueous layer was extracted with ether (×4), and the combined organic layers were washed with H2O (×2), 0.5N HCl (×2) and brine (×2), dried over MgSO4 and evaporated in vacuo. The crude product was purified by silica gel flash chromatography (5% EtOAc-95% hexanes) to provide the title compound as a colorless liquid (14 g). 1H NMR (CDCl3, 400 MHz) δ: 6.8-7.4 (4H), 5.8 (1H), 5.0 (2H), 3.83 (3H, OMe), 1.8-2.2 (4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06300316B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-a5d026940fd449d48e017e9c4e6a7526 |
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| Source note | uspto-grants-2001_10 |
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