HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 2-(3-Azabicyclo[3.1.0]hex-3-yl)-2-methylpropanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 1-(Dimethylamino)cyclopentanecarbonitrile | HCID 10773049 | — |
| Reactant | 3-Azabicyclo[3.1.0]hexane hydrochloride | HCID 22335289 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(3-Azabicyclo[3.1.0]hex-3-yl)-2-methylpropanenitrile | HCID 59347847 | 84% |
Reaction Steps
The title compound (583 mg, 84%) was prepared from 3-azabicyclo[3.1.0]hexane hydrochloride (550 mg, 4.6 mmol) [Pestic. Chem: Hum. Welfar Environ., Proc, Int, Congr. Pestic. Che., 5th, 1982, 1,159-64, 1983], acetone (267 mg, 4.6 mmol) and potassium cyanide (300 mg, 4.6 mmol) in water (2.5 ml) in a similar manner to that described in D1. 1H NMR (CDCl3) δ: 0.40 (1H, m), 0.58 (1H, m), 1.43 (8H, m), 2.64 (2H, m), 3.10 (2H, d, J=8 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745642B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-c1d6d633b3744333897c64fb2c8e38db |
| Source note | uspto-grants-2010_06 |