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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-OxetanamineHCID 9833923—
Reactant1-Bromo-4-iodo-2-methoxybenzeneHCID 12187202—
ReagentSodium t-butoxideHCID 23676156—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductN-(4-bromo-3-methoxyphenyl)oxetan-3-amineHCID 8285813235.77%

Reaction Conditions

Temperature80 °C

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 dataset750 AstraZeneca ELN dataset
ORD IDord-29003fa36fea4ddebef83b29dba29c7c
Source note750 AstraZeneca ELN dataset