Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 54055865 | HCID 54055865 | — |
| Catalyst | Hydrogen Bromide | HCID 260 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl acetate hexane acetic acid | HCID 21901998 | — |
| Product | HCID 54051922 | HCID 54051922 | — |
Reaction Steps
To a solution of 10.26 g. of 1-[3-(4-fluorobenzoyl)propionyl]-L-proline (Example 17) in 100 ml. of acetic acid is added 3 drops of 30% hydrogen bromide in acetic acid. A solution of 5.6 g. of bromine in 20 ml. of acetic acid is then added dropwise and the mixture is stirred at room temperature overnight. The mixture is evaporated to 1/3 its volume, poured into ice and water and extracted with dichloromethane. The organic extract is washed twice with water and then with saline, dried over magnesium sulfate and evaporated to dryness in vacuo with moderate heat, giving a white glass. This glass is scraped from the flask giving 12.2 g. of white powder. This powder is dissolved in ethyl acetate-hexane-acetic acid (75:25:2), placed on a 11/2"×20" silica gel column and eluted with the same solvent system, taking 100 ml. cuts with a 300 ml. fore-cut and a 400 ml. hold back volume. Cuts 2, 5 and 6 are combined and re-columned in the same manner. Cut 2 gives the desired product as 2.0 g. of a white glass.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04226775 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-e8d34f23356e4d979190ac2b9f6fb342 |
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| Source note | uspto-grants-1980_10 |
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