HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058266Generated: November 1, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 18672376, compound
https://huagongshe.com/reaction/1058266
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 69939028 | HCID 69939028 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18672376 | HCID 18672376 | — |
Reaction Steps
To a stirred solution of 2-(1-tert-butyloxycarbonylaminoethyl)-5-chlorobenzyl alcohol from the previous step (0.272 g, 0.96 mmol) in toluene (20.0 mL) at ambient temperature under nitrogen atmosphere was added DBU (0.15 mL g, 1.0 mmol) and DPPA (0.25 mL, 1.14 mmol). The mixture was stirred at ambient temperature for 18 h. The reaction was partitioned between EtOAc and water. The EtOAc layer was separated, dried over anhydrous Na2SO4, and filtered. The filtrate solvent was removed under reduced pressure and the residue purified by flash silica gel chromatography using dichloromethane as an eluent. 2-(1-(tert-butyloxycarbonylamino)ethyl)-5-chloro-benzylazide was obtained as a yellow oil after concentration of desired fractions in vacuo (0.28 g; HPLC RT 3.71 min, method A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06515011B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-31646af02a84418aaca50b77b1bdc393 |
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| Source note | uspto-grants-2003_02 |
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