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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509316Generated: October 30, 2026

Acetonitrile → 1-(4-Bromophenyl)-3,3-dimethoxycyclobutanamine

https://huagongshe.com/reaction/1509316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodiumHCID 5360545—
Reactant1-(4-Bromophenyl)-3,3-dimethoxycyclobutanecarboxamideHCID 67254266—
ReactantHCID 178525681HCID 178525681—
SolventWaterHCID 962—
Product1-(4-Bromophenyl)-3,3-dimethoxycyclobutanamineHCID 67257084—

Reaction Steps

To a solution of 1-(4-bromophenyl)-3,3-dimethoxycyclobutanecarboxamide (2.3 g, 7.32 mmol) in acetonitrile (9 ml) and Water (9.00 ml) was added phenyliodine bis(trifluoroacetate) (4.73 g, 11.00 mmol) and the resulting mixture was stirred at room temperature for 18 h. The reaction mixture was slowly poured into sodium bicarnate sat. solution (˜45 ml) and extracted with ethyl acetate (3×30 ml). The combined organic phase was washed with water, brine and concentrated to give crude product (3.4 g). The crude product was purified by column (biotage, 50 g) eluted with 0-5% DCM/Methanol (mixture of 500 ml methanol and 60 ml 2M NH4OH in methanol) to give product 1-(4-bromophenyl)-3,3-dimethoxycyclobutanamine (1.06 g), 1H NMR (500 MHz, CDCl3): 7.48 (d, 2H), 7.32 (d, 2H), 3.27 (d, 3H), 3.17 (d, 3H), 2.66 (d, 2H), 2.44 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221838B2
Source datasetuspto-grants-2015_12
ORD IDord-0080b0cb144e45159da1b468f2549838
Source noteuspto-grants-2015_12