HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066906Generated: October 30, 2026
Water → (1-Benzhydryl-azetidin-3-yl)-(2-methoxy-phenyl)-methyl-amine
https://huagongshe.com/reaction/1066906
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methoxy-N-methylaniline | HCID 2759579 | — |
| Reactant | 1-Benzhydryl-3-(methylsulfonyl)azetidine | HCID 15521969 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (1-Benzhydryl-azetidin-3-yl)-(2-methoxy-phenyl)-methyl-amine | HCID 21196806 | 25.9% |
Reaction Steps
To a solution of 0.65 g of N-methyl o-anisidine in 15 mL of acetonitrile, was added 0.280 g of K2CO3, followed by 0.650 g of 1-(diphenylmethyl)-3-methane sulfonyl azetidine. The reaction mixture was heated at 80° C. for 1 h then at 50° C. overnight. Water was added and the mixture was extracted with ether. The organic phase was dried and the solvent was removed under vacuo. The product was filtered through 100 mL of silica gel, eluting a with 15% ethyl acetate/hexanes then 25% ethyl acetate/hexanes to give 0.200 g of the desired product: mp 91-95° C. MS (ES) m/z (relative intensity): 356 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06245799B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-5e6e155447f34d639c8d0f88bb7dc6a9 |
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| Source note | uspto-grants-2001_06 |
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