HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → phenyl-Alanine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 10866487 | HCID 10866487 | — |
| Solvent | Potassium Cyanide | HCID 9032 | — |
| Product | phenyl-Alanine | HCID 817923 | 85% |
Reaction Steps
Following the same mode of operation as in the above example, starting with 0.14 g (approx. 10-3 mol) of α-hydroxyphenyl propionitrile in 2 ml of 0.1 M solution in KCN and 0.2 M in NH4OH 10 N, and after adding 0.06 g of acetone and 0.11 ml of NaOH 10 N after neutralisation, quantitative analysis by an analyst of α-amino acids gave a yield of 85% of phenyl alanine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04243814 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-f0497aef095141fb94ff8352effe82ef |
| Source note | uspto-grants-1981_01 |