HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetonitrile → 2-(4-oxopiperidin-1-yl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Piperonylamine | HCID 2723901 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-oxopiperidin-1-yl)acetonitrile | HCID 2760921 | — |
Reaction Steps
A suspension of 25.0 g of 4-piperidinone monohydrochloride monohydrate, 11.5 ml of chloroacetonitrile and 57.0 ml of diisopropylethylamine in 250 ml of tetrahydrofuran was refluxed for 10 hours. After the reaction, an insoluble matter was filtered off. The filtrate was added with saturated aqueous sodium hydrogencarbonate solution and extracted with a mixture of ethyl acetate and methanol (10:1). The extract was dried, and the solvent was evaporated to give brown crystals. The crystals were washed with a mixture of ethyl acetate and n-heptane to give 15.7 g of pale brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06518265B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-d96a4e9b8c024403a4170b9d176b4a83 |
| Source note | uspto-grants-2003_02 |