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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627Generated: October 25, 2026

2-Bromo-4-nitrotoluene → N-(2-methyl-5-nitrophenyl)oxetan-3-amine

https://huagongshe.com/reaction/627

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4-nitrotolueneHCID 82189—
ReactantOxetan-3-amine hydrochlorideHCID 23062080—
ReagentCesium carbonateHCID 10796—
CatalystPalladium (II) acetateHCID 4144353—
Catalyst(R)-(-)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldi-t-butylphosphine;Ferrocene, 1-[(1R)-1-[bis(1,1-dimethylethyl)phosphino]ethyl]-2-(dicyclohexylphosphino)-, (2R)-HCID 144543273—
ProductN-(2-methyl-5-nitrophenyl)oxetan-3-amineHCID 8049407928.82%

Reaction Conditions

Temperature90 °C

Reaction Steps

2-bromo-1-methyl-4-nitrobenzene (864 mg, 4mmol), oxetan-3-amine hydrochloride (438 mg, 4 mmol), CS2CO3 (3910 mg, 12.00 mmol), palladium(II) acetate (44.9 mg, 0.20 mmol), (R)-(-)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldi-t- butylphosphine (224 mg, 0.40 mmol) in 1,4-doxane was degased, inflated with Ar and heated at 90 oC for 5h. LCMS showed some product peak. Silica gel 2g was added to the mixture, evaporated all solvents in GeneVac. The sample was dry loaded for purification by ISCO (Hexane/EtOAc=100/10-100/50) N-(2-methyl-5-nitrophenyl)oxetan-3-amine (240 mg, 28.8 %) 1H NMR (400 MHz, CD2Cl2) d: 7.47 (dd, 1H), 7.14 (d, 1H), 6.98 (s, 1H), 4.99 (t, 2H), 4.63 (m, 1H), 4.46 (t, 2H), 4.20(m, 1H), 2.18 (s, 3H). LCMS: 209 [M+H]+.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-85488250153944e595f74578eeba1555
Source note750 AstraZeneca ELN dataset