HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522931Generated: October 30, 2026
Toluene → 1-(3-Bromophenyl)-3-(4-fluorophenoxy)azetidine
https://huagongshe.com/reaction/522931
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1,3-Dibromobenzene | HCID 7927 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 3-(4-Fluorophenoxy)azetidine | HCID 21428730 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | 1-(3-Bromophenyl)-3-(4-fluorophenoxy)azetidine | HCID 67354815 | 30% |
Reaction Steps
To a solution of 1, 3-dibromobenzene (500 mg, 2.13 mmol) and 3-(4-fluorophenoxy)azetidine (357 mg, 2.13 mmol) in toluene (7 mL, 3 mmol) was added cesium carbonate (600 mg, 5.3 mmol) and degassed for 15 min. Pd2(dba)3 (97 mg, 0.106 mmol) and BINAP (66 mg, 0.106 mmol) were added and the mixture was heated in the microwave for 30 min at 100° C. The reaction mixture was concentrated under reduced pressure and extracted with EtOAc (2×30 mL). The organic extracts were washed with brine, dried over sodium sulfate and concentrated under reduced pressure. Purification by silica gel column chromatography provided 1-(3-bromophenyl)-3-(4-fluorophenoxy)azetidine (200 mg, 30%) as a solid. Observed mass (M+1): 322.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334269B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-8885093045b5433bb7d6a5a19411150c |
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| Source note | uspto-grants-2016_05 |
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