HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5970Generated: October 26, 2026
Lithium azide → 2-(2-(((1,1-Dimethylethyl)dimethylsilyl)oxy)ethyl)-3-(((1,1-dimethylethyl)dimethylsilyl)oxymethyl)-1-azidocyclobutane
https://huagongshe.com/reaction/5970
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium azide | HCID 88163 | — |
| Reactant | 2-(((1,1-Dimethylethyl)dimethylsilyl)oxy)ethyl-3-(((1,1-dimethylethyl)dimethyl-silyl)oxymethyl)-1-O-methanesulfonylcyclobutanol | HCID 86747236 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-(((1,1-Dimethylethyl)dimethylsilyl)oxy)ethyl)-3-(((1,1-dimethylethyl)dimethylsilyl)oxymethyl)-1-azidocyclobutane | HCID 19794250 | 146.4% |
Reaction Steps
2-(2-(((1,1-Dimethylethyl)dimethylsilyl)oxy)ethyl-3-(((1,1-dimethylethyl)dimethyl-silyl)oxymethyl)-1-O-methanesulfonylcyclobutanol (180 mg, 0.41 mmol) was mixed with 200 mg (4.1 mmol) of lithium azide in 4 mL of DMF. The reaction mixture was heated at 80° C. for 2 h then concentrated in vacuo. The residue was purified on a silica gel column eluted with 5% ethyl acetate in hexane to give 120 mg (73% yield) of the title compound; MS DCI-NH3M/Z: 400 (M+H)+, 417 (M+NH4)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05246931 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-d5f0c7a4ccb444f19b70b9728ca3aa5e |
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| Source note | uspto-grants-1993_09 |
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