HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 11065077, compound → Gabapentin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 11065077 | HCID 11065077 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Rhodium | HCID 23948 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Gabapentin | HCID 3446 | 27.7% |
Reaction Steps
1.0 g (3.8 mmol) of (1-cyanocyclohexyl)acetic acid benzyl ester was distilled in 20 ml of methanol, mixed with 0.2 g of Rh/C 5 percent and hydrogenated at 10 bars of hydrogen pressure. After 23 hours at room temperature the suspension was filtered, the filtrate was concentrated to 3 ml, mixed with 25 ml of ethanol, concentrated to 4 ml and put on the cooling shelf. The precipitated product was filtered, washed with ethanol and dried. 0.18 g of Gabapentin was obtained, corresponding to a yield of 27 percent (relative to the (1-cyanocyclohexyl)acetic acid benzyl ester used). Data for the product was:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05130455 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-23ab3efe560a4067a7d9ef8ac6253643 |
| Source note | uspto-grants-1992_07 |