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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 1-(4-Bromophenyl)-3,3-dimethoxycyclobutanecarboxamide | HCID 67254266 | — |
| Reactant | HCID 178525681 | HCID 178525681 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(4-Bromophenyl)-3,3-dimethoxycyclobutanamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221838B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-0080b0cb144e45159da1b468f2549838 |
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| Source note | uspto-grants-2015_12 |
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