HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47043Generated: October 25, 2026
Hydrogen Bromide → L-alanyl-L-proline ethylamide hydrobromide
https://huagongshe.com/reaction/47043
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | N-benzyloxycarbonyl-L-alanyl-L-proline ethylamide | HCID 13749998 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | L-alanyl-L-proline ethylamide hydrobromide | HCID 70602162 | 82% |
Reaction Steps
1.81 g (0.0052 mol) of N-benzyloxycarbonyl-L-alanyl-L-proline ethylamide were stirred for 1 hour in 10 ml of 4-N hydrobromic acid in acetic acid. To the solution were added 150 ml of dry ether and, after stirring for a few minutes, the oil was allowed to settle. The mixture was cooled to -60° C. and the ether decanted from the oil and discarded. The oil was then dissolved in methanol, the product crystallising out on the addition of ethyl acetate. There were obtained 1.25 g (82%) of L-alanyl-L-proline ethylamide hydrobromide of melting point 202°-204° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04176116 |
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| Source dataset | uspto-grants-1979_11 |
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| ORD ID | ord-83dee15e6ad243779612f1005e1fd9b0 |
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| Source note | uspto-grants-1979_11 |
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