HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 1-[3-Acetylthio-3-(4-bromobenzoyl)propionyl]-L-proline methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Reactant | 1-[3-(4-Bromobenzoyl)-3-bromopropionyl]-L-proline methyl ester | HCID 54138682 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-[3-Acetylthio-3-(4-bromobenzoyl)propionyl]-L-proline methyl ester | HCID 54216506 | — |
Reaction Steps
To a solution of 5.28 g. of 1-[3-(4-bromobenzoyl)-3-bromopropionyl)-L-proline methyl ester (Example 30) in 35 ml. of acetonitrile is added 1.48 g. of potassium thioacetate. The mixture is stirred at room temperature for 2 hours, filtered and the filtrate is evaporated to dryness in vacuo leaving an amber gum. This is dissolved in ether and chromatographed on a 1"×16" silica gel column, eluting with ether and taking 100 ml. cuts. Cut number 3 gives the desired product (1.64 g.) as a glass.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04226775 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-b72709c3f8aa401591ce49aa194fa727 |
| Source note | uspto-grants-1980_10 |