HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721374Generated: October 31, 2026
Triethylamine → 1-(Diphenylmethyl)azetidin-3-one
https://huagongshe.com/reaction/1721374
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(Diphenylmethyl)azetidin-3-ol | HCID 330448 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-(Diphenylmethyl)azetidin-3-one | HCID 3735558 | 98.8% |
Reaction Steps
Triethylamine (112.1 g, 1.11 mols) was added to a solution of N-diphenylmethylazetidin-3-ol (26.6 g, 0.11 mol) in DMSO (300 ml). The solution was cooled to 10° C. and a solution of sulphur trioxide-pyridine complex (112 g, 0.7 mol) in DMSO (500 ml) added, rapidly. Stirring was continued at 10° C. for 0.75h and the mixture then warmed to 25° C. and stirred for 1h. The solution was poured into ice-water (21) and extracted with EtOAc (3×1). The combined extracts were washed with water (500 ml) and brine (500 ml) and dried (Na2SO4). The crude product was purified by chromatography through silica-gel eluting with petroleum ether/EtOAc (2:1) to give the desired ketone (25.8 g), mp 74°-75° C.; δ (360 MHz, CDCl3) 4.00 (4H, s, 2 of CH2), 4.59 (1H, s, CH), 7.19-7.49 (10H, m, Ar--H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05510362 |
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| Source dataset | uspto-grants-1996_04 |
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| ORD ID | ord-971f180f4b9f44bbb02e7f40b5028498 |
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| Source note | uspto-grants-1996_04 |
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