HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307222Generated: November 2, 2026
Methanesulfonyl chloride → HCID 22605405, compound
https://huagongshe.com/reaction/2307222
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 53767266 | HCID 53767266 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22605405 | HCID 22605405 | — |
Reaction Steps
To a stirred solution of 3-(4-fluorophenyl)-1-diphenylmethyl-3-azetidinol (15) (4.0 g) and N,N-diisopropylethylamine (3.2 mL) in dichloromethane (100 mL) at 0° C. was added, dropwise, methanesulfonyl chloride (125 mL). The mixture was stirred at 0° C. for 18 hrs, then washed (water, brine) and dried (Na2SO4) and concentrated in vacuo. The crude product was recrystallised from hexane to give 3-(4-fluorophenyl)-3-chloro-1-(diphenylmethyl)azetidine (16) (22 g), m.p. 108-109° C. (hexane). Found: C, 75.13; H, 5.46; N, 3.93. C22H19CIFN C, 75.10; H, 5.44; N, 3.98%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06831078B1 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-bafba58ab5c640f4b9df5d0192c1a98e |
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| Source note | uspto-grants-2004_12 |
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