HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911627Generated: November 1, 2026
HCID 57656058, compound → HCID 57655921, compound
https://huagongshe.com/reaction/911627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57656058 | HCID 57656058 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57655921 | HCID 57655921 | 94% |
Reaction Steps
Combine a solution of (R)-4-cyano-2-fluoro-N-(2,2,2-trifluoro-1-methyl-ethyl)-benzamide (0.904 g, 3.475 mmol) in absolute ethanol (26 mL), water (9.7 mL) and glacial acetic acid (1.2 mL) with 10% Pd/C (Degussa type E101, 0.27 g, 0.13 mmol) under nitrogen. Purge the mixture with nitrogen and then with hydrogen. Stir the slurry at room temperature under hydrogen at 55 psi for 30 min. Purge the reaction mixture with nitrogen and then filter the slurry over Celite®. Wash the filter cake with ethanol (100 mL) and THF (100 mL). Concentrate the filtrate and purify by SCX chromatography eluting with dichloromethane/methanol (1:1) to remove impurities and then with dichloromethane/2M ammonia in methanol (1:1) to elute product. Concentrate to afford the title compound as a colorless oil (0.86 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08022062B2 |
|---|
| Source dataset | uspto-grants-2011_09 |
|---|
| ORD ID | ord-79d940d4b4ed408194b09cddc34dc8e9 |
|---|
| Source note | uspto-grants-2011_09 |
|---|