HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632Generated: October 26, 2026
3-Oxetanamine → N-(4-bromo-3-methoxyphenyl)oxetan-3-amine
https://huagongshe.com/reaction/632
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Oxetanamine | HCID 9833923 | — |
| Reactant | 1-Bromo-4-iodo-2-methoxybenzene | HCID 12187202 | — |
| Reagent | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(4-bromo-3-methoxyphenyl)oxetan-3-amine | HCID 82858132 | 35.77% |
Reaction Steps
A solution of 1-bromo-4-iodo-2-methoxybenzene (0.60 g, 1.92 mmol) dissolved in toluene (15 mL) was treated with oxetan-3-amine (0.140 g, 1.92 mmol), SODIUM TERT-BUTOXIDE (0.221 g, 2.30 mmol), XANTPHOS (0.111 g, 0.19 mmol) and TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (0.044 g, 0.05 mmol) under nitrogen. The resulting mixture was stirred at 80 °C in a sealed tube for 2 hours. The reaction mixture was diluted with water (10 mL), and extracted with ethyl acetate (3x 20 mL). The organic was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution 0-30% EtOAc in Heptane. Pure fractions were evaporated to dryness to afford N-(4-bromo-3-methoxyphenyl)oxetan-3-amine (0.177 g, 35.8 %) as a beige solid.
Provenance & Evidence
| Source dataset | 750 AstraZeneca ELN dataset |
|---|
| ORD ID | ord-29003fa36fea4ddebef83b29dba29c7c |
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| Source note | 750 AstraZeneca ELN dataset |
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