HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Thioadenosine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | HCID 53795338 | HCID 53795338 | — |
| Product | 2-Thioadenosine | HCID 6451965 | 76% |
Reaction Steps
0.45 g of 5-amino-1-β-D-ribofuranosylimidazole-4-carboxamide O-(p-methylbenzyl)-oxime was dissolved in 8 ml of an aqueous solution containing 1 ml of ethanol, and 2 ml of carbon disulfide was added to the solution. The resulting mixture was allowed to react in an autoclave at 130° C for 5 hours under autogenous pressure (about 10 Kg/cm2), and the reaction product was worked up in the same manner as described in Example 1 to obtain 0.288 g of 2-thioadenosine having a melting point of 198° C (with decomposition) in a 76% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03989682 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-85f2ecd6fb614c7faf0d3ad7f6fea081 |
| Source note | uspto-grants-1976_11 |