HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromoheptane → Eptastigmine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromoheptane | HCID 12369 | — |
| Reactant | Eseroline | HCID 119198 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Catalyst | Tetraethylammonium Bromide | HCID 6285 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Eptastigmine | HCID 65872 | 63% |
Reaction Steps
150 g of eseroline (0.69 mole), 83.9 g of potassium cyanate (1.035 moles), 148 g of 1-bromoheptane (0.83 mole) and 29 g of tetraethylammonium bromide (0.14 mole) are placed into 5 l of anhydrous acetonitrile. The reaction mixture is refluxed for 19 hours, the insolubles are filtered off and the mixture is worked up as described in Example 1. Heptastigmine yield is 63%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705657 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-6c619a3576e14e828e081d3f7faa104b |
| Source note | uspto-grants-1998_01 |