HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → L-Phenylalanine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Phenylacetaldehyde | HCID 998 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Ammonium Carbonate | HCID 517111 | — |
| Reactant | Potassium Bisulfite | HCID 23663620 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | L-Phenylalanine | HCID 6140 | — |
Reaction Steps
In a 100 l-volume hasteroi-made autoclave was placed 7.2 kg (30 moles) of a potassium bisulfite addition salt of phenylacetaldehyde, 1.76 kg (35.9 moles) of sodium cyanide, 4.32 kg (45 mole) of ammonium carbonate, 6 l (90 mole) of a 25% aqueous ammonia, 9 l of methanol and 24 l of water and the mixture was reacted at 100° C. for 2 hours to obtain precursors of phenylalanine. After the ammonia and methanol were removed by heating the reaction solution, the hydrolysis was carried out at 150° C. for 1.0 hour using 4.8 kg (120 moles) of caustic soda.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04549028 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-5ed97fdd202f42ffa05e2d7fc2adfb18 |
| Source note | uspto-grants-1985_10 |