HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 3-Carbobenzoxyamino-2-hydroxy-5-methylhexanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | N-carbobenzoxy-L-leucinal | HCID 10911911 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Carbobenzoxyamino-2-hydroxy-5-methylhexanenitrile | HCID 13848629 | 81.6% |
Reaction Steps
A solution of 3.43 g of sodium bisulfite in 20 ml of water was added to 2.81 g of N-carbobenzoxy-L-leucinal, and the mixture was stirred under ice-cooling for 14 hours. To the reaction mixture were added a solution of 1.41 g of potassium cyanide in 50 ml of water and 200 ml of ethyl acetate, and the mixture was stirred at room temperature for 4 hours. The ethyl acetate layer was washed with a saturated sodium chloride aqueous solution, dried over magnesium sulfate, and concentrated under reduced pressure to obtain 2.54 g of 3-carbobenzoxyamino-2-hydroxy-5-methylhexanenitrile as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04857650 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-ee593498200d4266a9b6d9e461d60221 |
| Source note | uspto-grants-1989_08 |