HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68697Generated: October 28, 2026
Methanesulfonyl chloride → HCID 86658770, compound
https://huagongshe.com/reaction/68697
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Tert-butyl 4-(3-hydroxyazetidin-1-yl)piperidine-1-carboxylate | HCID 50986422 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86658770 | HCID 86658770 | — |
Reaction Steps
Into a 100-mL 3-necked round-bottom flask, was placed a solution of tert-butyl 4-(3-hydroxyazetidin-1-yl)piperidine-1-carboxylate (300 mg, 1.15 mmol, 1.00 equiv, 98%) in dichloromethane (20 mL), TEA (240 mg, 2.33 mmol, 2.00 equiv, 98%). To the resulting mixture was added MsCl (0.6 mg, 0.01 mmol, 4.50 equiv, 98%) dropwise with stirring. The resulting solution was stirred for 2 h at room temperature in an ice/salt bath. The reaction was then quenched by the addition of water. The resulting solution was extracted with dichloromethane (2×50 mL) and the organic layers combined. The resulting mixture was washed with sodium chloride/H2O (1×100 mL). The resulting mixture was dried over anhydrous sodium sulfate and concentrated under vacuum to yield tert-butyl 4-(3-(methylsulfonyloxy)azetidin-1-yl)piperidine-1-carboxylate as a white solid. MS: 335 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822447B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-714c3cf17674465bbcc277d634dc30c4 |
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| Source note | uspto-grants-2014_09 |
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