HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → 4-Aminothiane-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tetrahydrothiopyran-4-one | HCID 66173 | — |
| Product | 4-Aminothiane-4-carbonitrile | HCID 15818740 | — |
Reaction Steps
Using the procedure of Stage 1 of Example 1, 8 ml of ammonium hydroxide, 1.58 g of ammonium chloride, 1.23 g of sodium cyanide and 2.51 g of tetrahydro-4H-thiopyran-4-one were reacted and the mixture was stirred for 18 hours at ambient temperature. Extraction was carried out 3 times with methylene chloride, followed by washing with salt water and drying to obtain 2.88 g of the expected product (white crystals) melting at 51-52° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05958936 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-a20e9eee7edf4a0bbdc099b9b8391398 |
| Source note | uspto-grants-1999_09 |