HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 20311570, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 2-(Phenylamino)acetamide | HCID 15370319 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20311570 | HCID 20311570 | — |
Reaction Steps
To a mixture of 3.75 g. of anilinoacetamide, 2.5 g. of potassium bicarbonate and 50 ml. of ethanol was added rapidly 2.7 g. of cyanogen bromide in 20 ml. of ethanol. The reaction mixture was heated to reflux. After heating overnight and cooling, a small amount of precipitate was in the flask. This was filtered and the ethanolic filtrate shown to be slightly acidic. The ethanol filtrate was concentrated down to dryness leaving a solid which was washed with ethanol. The yield of product, m.p. 117°-9° C., was 3.9 g. (88%). The mass spectrum of the product gives a parent ion at m/e 175. This product is used to prepare intermediate III.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04110445 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-f189126fe418449f9944debf2dc4c410 |
| Source note | uspto-grants-1978_08 |