HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → L-phenylalanine methyl ester sulfate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | L-Phenylalanine | HCID 6140 | — |
| Product | L-phenylalanine methyl ester sulfate | HCID 20841682 | 66.7% |
Reaction Steps
The same esterification procedure as in Example 1 was followed with the exception that 165.2 g of L-phenylalanine and 165.2 g of methanol were used and that the hydrochloric acid was replaced with 120.1 g of 98% sulfuric acid. The reaction was conducted at 60° C. for 8 hours, followed by cooling in order to deposit the crystals, which were collected by filtration and then dried to obtain 184.9 g (63.8% yield) of L-phenylalanine methyl ester sulfate having a purity of 95.7% and containing 0.3% of water and 2.4% of L-phenylalanine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05113009 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-1ab463adca39436ab0eec024eae6ef11 |
| Source note | uspto-grants-1992_05 |