HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601681Generated: October 30, 2026
Triethylamine → 3-Methoxy-cyclobutylmethylazide
https://huagongshe.com/reaction/601681
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | (3-Methoxycyclobutyl)methanol | HCID 23158380 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Methoxy-cyclobutylmethylazide | HCID 23158335 | 72.9% |
Reaction Steps
530 μl of triethylamine followed by 220 μl of methanesulfonylchloride were added under iced temperature to 220 mg of 1) 3-methoxy-cyclobutylmethanol obtained in the above 1). The mixture was heated to room temperature and stirred for 30 min. The reaction solution was diluted with ethyl acetate, washed with water, saturated sodium bicarbonate water and saturated saline solution, and dried with anhydrous sodium sulfate. The residues obtained by evaportating the solvents under reduced pressure were dissolved in 4 ml of dimethylformamide. Then, 245 mg of sodium azide was added, and the mixture was stirred at 80° C. for 1.5 hours. The reaction solution was diluted with ethyl acetate, washed with water and saturated saline solution and dried with anhydrous sodium sulfate. The residues obtained by distilling out the solvents under reduced pressure were separated and purified by silicagel column chromatography (ethyl acetate:hexane=10:90) to obtain 195 mg of the above compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902369B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-bf530e4ce0074f84884d1ad667b1d969 |
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| Source note | uspto-grants-2011_03 |
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