HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(2-Chloroacetyl)piperidine-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Cyanopiperidine | HCID 138223 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-Chloroacetyl)piperidine-4-carbonitrile | HCID 67470097 | — |
Reaction Steps
Chloroacetyl chloride (0.43 mL) was added to a mixture of a solution of 4-cyanopiperidine (500 mg) in CH2Cl2 (5 mL) and an aqueous 2 M Na2CO3 solution (5.7 mL) under ice-cooling, and the mixture was stirred for 30 minutes under ice-cooling. After the reaction mixture was further stirred at room temperature for 4 hours, CH2Cl2 and water were added thereto, then, extraction was performed on the mixture using CH2Cl2, and the extract was washed with saturated brine. The organic layer was dried over Na2SO4 and filtered, and the filtrate was concentrated under reduced pressure, whereby 1-(chloroacetyl)piperidine-4-carbonitrile (845 mg) was obtained as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09328118B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-f2ce59af567a4253bd30cedbd9234afe |
| Source note | uspto-grants-2016_05 |