HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 6-oxopiperidine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 6-Oxopiperidine-3-carboxylic acid | HCID 560090 | — |
| Product | Ethyl 6-oxopiperidine-3-carboxylate | HCID 15386078 | — |
Reaction Steps
To a suspension of 250 g of 5-carboxy-2-piperidone in 2.5 liters of punctilious ethanol were added 500 g of thionyl chloride at 22° C. Stir for 18 hours. The resulting solution was evaporated to dryness and the residue triturated with ether to give 233 g of the title compound: MS m/z 171 (M+), 142, 126, 115, 98; 300-MHz 1H NMR (DMSO-d6) δ1.21 (t, J=7 Hz, 3 H), 1.78-1.92 (m, 1 H), 1.95-2.08 (m, 1 H), 2.15-2.31 (m, 2 H), 2.78-2.89 (m, 1 H), 3.25-3.40 (m, 2 H), 4.12 (t, J=7 Hz, 2 H), 7.95 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05159079 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-a3419a3ade9f4219a19bd7dad1d0bd3e |
| Source note | uspto-grants-1992_10 |