Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 13389842 | HCID 13389842 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Product | HCID 18602836 | HCID 18602836 | 96% |
Reaction Steps
N-t-butyloxycarbonyl-L-alanyl-N-(2-indanyl) glycyl-L-proline benzylester (2.72 g, 4.95 m mole) was dissolved in 4N hydrogen chloride dioxane solution (50 ml) and the mixture was stirred for 1 hour at room temperature. The solvent was distilled off under reduced pressure from the solution, and thereby a sticky residue was obtained. The residue was made into a crystalline form by the addition of ethyl ether, and the crystal was obtained on the filter paper, and immediately dried in the desiccator to obtain a white powder of L-alanyl-N-(2-indanyl) glycyl-L-proline benzylester hydrochloride (2.31 g, 4.76 m mole, yield: 96%). This product had a hygrospic nature, and gave a single spot with Rf =0.42 by silica gel thin layer chromatography (developing solvent, chloroform:methanol:triethylamine=40:2:1, Colour forming method: spraying of 0.1% ninhydrin and heating).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04536395 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-8f5c3e596fc6453eb09a0dd3ecd534b0 |
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| Source note | uspto-grants-1985_08 |
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