Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Bicarbonate | HCID 14013 | — |
| Reactant | N-(2-Chloroacetyl)-L-tyrosine | HCID 2724332 | — |
| Solvent | Ammonia | HCID 222 | — |
| Solvent | Water | HCID 962 | — |
| Product | Glycyl-L-tyrosine | HCID 92829 | — |
Reaction Steps
Ammonium hydrogencarbonate (1289 g) was dissolved in a mixture of 4000 ml of 28% aqueous ammonia and 1000 ml of distilled water at 35° C. To the solution were added 700 g (2.72 mol) of N-chloroacetyl-L-tyrosine and 700 ml of distilled water, followed by stirring at 40° C. for 5 hours. The reaction mixture was concentrated under reduced pressure to remove excess ammonia and then adjusted to pH 5.5 with concentrated hydrochloric acid at 45° C., followed by gradual cooling. After crystals were deposited, the mixture was ice-cooled and the crystals were isolated by filtration to give 600 g (489 g on anhydrous basis, 2.05 mol, 75.4%) of crude crystals of N-glycyl-L-tyrosine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06197998B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-30c8d1b2f7a44c748de54590ed461828 |
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| Source note | uspto-grants-2001_03 |
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