Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 57283447 | HCID 57283447 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67908176 | HCID 67908176 | — |
Reaction Steps
A mixture of 1 g of the product of Example 2, 8 ml of demineralized water and 0.8 ml of hydrochloric acid was stirred at 20° C. for one hour and was then heated at 60° C. for one hour and was cooled at 20° C. The mixture was diluted with 15 ml of water and was then extracted with methylene chloride. The organic phase was washed with aqueous N sodium hydroxide solution and with water until the wash water was neutral, dried and evaporated to dryness under reduced pressure. The residue was taken up in 10 ml of ether and a stream of hydrogen chloride was slowly bubbled therethrough. The mixture was vacuum filtered to obtain 350 mg of benzyl L-leucine hydrochloride melting at 135° C. and having a specific rotation of [α]D20 =-5.5°±1° (c=1% in 0.1 N hydrochloric acid). Circular Dichroism (dioxane): max. at 219 nm; Δε=+1.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04350637 |
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| Source dataset | uspto-grants-1982_09 |
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| ORD ID | ord-21d420eff18247d389c97da2dca27c1c |
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| Source note | uspto-grants-1982_09 |
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