HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetyl chloride → 1-(2-Chloroacetyl)piperidine-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Cyanopiperidine | HCID 138223 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(2-Chloroacetyl)piperidine-4-carbonitrile | HCID 67470097 | 92.9% |
Reaction Conditions
| Temperature | -10 °C |
|---|
Reaction Steps
A mixture of 4-piperidinecarbonitrile (200 g, 1.80 mol) and 40% aqueous potassium carbonate solution (342 g, 0.99 mol) in dichloromethane (1 L) was cooled to −10° C., and a solution of chloroacetyl chloride (210 g, 1.86 mol) in dichloromethane (300 mL) was added over about 75 minutes while maintaining the reaction mixture at −10 to 0° C. After the addition was complete, the reaction mixture was separated, the upper aqueous phase was extracted with dichloromethane (2×300 mL), and the combined organic phases were concentrated under reduced pressure to give 312 g of the title compound as a liquid which slowly crystallized on standing. This compound was of sufficient purity to use in subsequent reactions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722678B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-7e23b385b08f45b3840ed4d253a51158 |
| Source note | uspto-grants-2014_05 |