HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Ethyl 5-(1-benzyloxycarbonyl-4-piperidyl)valerate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-(1-Benzyloxycarbonyl-4-piperidyl)valeric acid | HCID 20143722 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 5-(1-benzyloxycarbonyl-4-piperidyl)valerate | HCID 14046929 | — |
Reaction Steps
A mixture of 5-(1-benzyloxycarbonyl-4-piperidyl)valeric acid (54.8 g), sodium bicarbonate (29 g), ethyl iodide (21 ml) and N,N-dimethylformamide (150 ml) is stirred for 3 hours at 70°-80° C. After further addition of ethyl iodide (10 ml), the stirring is continued for further 3 hours at 90°-100° C. After cooling, the mixture is diluted with water and extracted with ethyl acetate (1 l). The extract is washed successively with water, 1N hydrochloric acid and sodium bicarbonate solution, dried over anhydrous magnesium sulfate and evaporated in vacuo to yield ethyl 5-(1-benzyloxycarbonyl-4-piperidyl)valerate (58 g) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04591458 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-64bdf880f2f44400ab9b2d2427ec7b46 |
| Source note | uspto-grants-1986_05 |