HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712645Generated: November 1, 2026
Water → 1-(Diphenylmethyl)azetidine-3-carbonitrile
https://huagongshe.com/reaction/1712645
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Cyanate | HCID 517096 | — |
| Reactant | 1-(Diphenylmethyl)azetidin-3-yl methanesulfonate | HCID 2758716 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(Diphenylmethyl)azetidine-3-carbonitrile | HCID 2779290 | 92.3% |
Reaction Steps
Water (7.2 ml) and sodium cyanate (3.48 g) were added to a solution of 1-benzhydryl-3-(methanesulfonyloxy)azetidine (7.52 g) in N,N-dimethylformamide (60 ml), followed by stirring at 65° C. for 9 hours. Water, sodium carbonate and ethyl acetate were added to the reaction mixture, which was partitioned. The aqueous layer was extracted with ethyl acetate. The organic layer was collected, washed with brine, and dried over anhydrous sodium sulfate. This was concentrated under reduced pressure, and the resultant crystals were suspended by addition of diethyl ether (10 ml). The crystals were collected by filtration, and washed with diethyl ether. This was dried under aeration to give the title compound (5.43 g, 92.3%) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07790885B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-ad9a7ef4b7a544ff9a39404133548214 |
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| Source note | uspto-grants-2010_09 |
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