HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739743Generated: October 30, 2026
Water → 4-[1-(Diphenylmethyl)azetidin-3-yl]morpholine
https://huagongshe.com/reaction/1739743
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Diphenylmethyl)azetidin-3-yl methanesulfonate | HCID 2758716 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-[1-(Diphenylmethyl)azetidin-3-yl]morpholine | HCID 21183786 | 693% |
Reaction Steps
A solution of 1-diphenylmethyl-3-methanesulphonyloxyazetidine (see Preparation 54) (24.46 g, 7.72 mmol), potassium carbonate (32 g, 3 mol. equiv.) and morpholine (7.34 ml, 1.09 mol. equiv.) in acetonitrile (200 ml) was heated under reflux for four hours. The solution was then cooled to room temperature, water (50 ml) added and the mixture concentrated under reduced pressure. The residue was partitioned between ethyl acetate (400 ml) and water (400 ml) and the organic phase separated and washed with water (2×400 ml). The organic phase was dried over magnesium sulphate, filtered and the solvent removed from the filtrate under reduced pressure. The residue was then chromatographed using silica gel eluting with hexane:diethyl ether (1:1, by volume) to give the title compound (16.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05968923 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-9b323fc69acd4a1b8480978216809ff0 |
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| Source note | uspto-grants-1999_10 |
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