HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl 3-(octahydroquinolin-1-yl)-3-oxopropionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Decahydroquinoline | HCID 92911 | — |
| Reactant | Ethyl 3-chloro-3-oxopropionate | HCID 118931 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 3-(octahydroquinolin-1-yl)-3-oxopropionate | HCID 66794569 | — |
Reaction Steps
3.38 mL of Et3N and 1.44 mL (11 mmol) of ethyl 3-chloro-3-oxopropionate are added to a solution of 1.5 mL (10 mmol) of decahydroquinoline in 100 mL of AcOEt. The resulting solution is kept under stirring at reflux for 10 h. Then water is added and the organic phase is separated, the aqueous phase is extracted once again with AcOEt. The organic phases are pooled and they are first washed with 5% solution of NaHCO3 and subsequently with brine, they are dried over anhydrous
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524894B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-7b31eb19252f4fb084552a23f4201ee8 |
| Source note | uspto-grants-2013_09 |