HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(benzyloxycarbonylamino)-N-(2-bromoethyl)propionamide → 3-(Benzyloxycarbonylamino)-N-[2-(benzoylthio)ethyl]propionamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(benzyloxycarbonylamino)-N-(2-bromoethyl)propionamide | HCID 20258752 | — |
| Reactant | Potassium thiobenzoate | HCID 23681850 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-(Benzyloxycarbonylamino)-N-[2-(benzoylthio)ethyl]propionamide | HCID 13491994 | 68.1% |
Reaction Steps
To the solution of 3-(benzyloxycarbonylamino)-N-(2-bromoethyl)propionamide (10.0 g, 0.03 mol) in acetone (250 ml), acetone (100 ml) solution of potassium thiobenzoate (5.35 g, 0.03 mol) is added. The mixture is stirred for 1 hour and insoluble substance is filtered off. The filtrate is concentrated in vacuo and the residue is dissolved in chloroform. The solution is washed with sodium hydroxide solution, water and then saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. The solution is concentrated in vacuo to give 7.9 g (68%) of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04552765 |
| Source dataset | uspto-grants-1985_11 |
| ORD ID | ord-9ed9e6b582544b2db1b97b798496dd4c |
| Source note | uspto-grants-1985_11 |