HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041963Generated: October 26, 2026
2-tert-Butylaniline → 1-benzhydryl-N-(2-tert-butylphenyl)azetidin-3-amine
https://huagongshe.com/reaction/2041963
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-tert-Butylaniline | HCID 80574 | — |
| Reactant | (1-Benzhydrylazetidin-3-yl)methanesulfonate | HCID 71431707 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-benzhydryl-N-(2-tert-butylphenyl)azetidin-3-amine | HCID 59577222 | 59% |
Reaction Steps
A mixture of 2-tert-butylaniline (0.50 g, 3.35 mmol) and 1-(diphenylmethyl)-3-azetidinylmethanesulfonate (1.60 g, 5.03 mmol) was heated at 100° C. for 15 min. After this toluene (5.0 ml) was added to the resulting yellow solid, the reaction mixture was cooled to room temperature, partitioned between THF and water and separated. The organic layer was washed with saturated sodium chloride, dried (Na2SO4), filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, 90:10 to 80:20 heptane/ethyl acetate) to provide 1-benzhydryl-N-(2-tert-butylphenyl)azetidin-3-amine (0.73 g, 59%) as a yellow gum-like substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586571B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-7f88933db6584281babab1af5e44a571 |
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| Source note | uspto-grants-2013_11 |
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