HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271504Generated: October 30, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → 4-[Azido-(5-methylfuran-2-yl)methyl]tetrahydropyran
https://huagongshe.com/reaction/2271504
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | (5-Methylfuran-2-yl)-(tetrahydropyran-4-yl)methanol | HCID 63937679 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-[Azido-(5-methylfuran-2-yl)methyl]tetrahydropyran | HCID 89525435 | 70% |
Reaction Steps
6.08 g (22 mmol, 1.1 eq) of diphenylphosphoryl azide were added dropwise to a solution of 4.43 g (20 mmol, 1 eq) of (5-methylfuran-2-yl)-(tetrahydropyran-4-yl)methanol at 89% in 60 ml of toluene. The reaction medium was cooled to 0° C. and then 3.3 ml (22 mmol, 1.1 eq) of 1,8-diazabicyclo[5.4.0]undec-7-ene were added dropwise. The reaction medium was stirred at ambient temperature for 22 hours. The reaction medium was separated by settling out and the organic phase was washed with water and then with 1 N hydrochloric acid, dried over magnesium sulfate, filtered and evaporated. The residue was chromatographed on silica gel (column Analogix SF40-240 g, Spot II) eluted with heptane/ethyl acetate (95/5). 3.09 g of 4-[azido-(5-methylfuran-2-yl)methyl]tetrahydropyran were obtained. Yield=70%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09120772B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-fb9881ffad204637ac2b5dff242c6948 |
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| Source note | uspto-grants-2015_09 |
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