HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → (3RS)-2-[(n-Butylthio)thiocarbonyl]-1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,2,3,4-Tetrahydro-Beta-Carboline-3-Carboxylic Acid | HCID 98285 | — |
| Product | (3RS)-2-[(n-Butylthio)thiocarbonyl]-1,2,3,4-tetrahydro-beta-carboline-3-carboxylic acid | HCID 13561924 | — |
Reaction Steps
In the same manner as described in Example 6, (3RS)-1,2,3,4-tetrahydro-β-carboline-3-carboxylic acid (3.24 g), KOH (96%, 1.75 g), 50% ethanol (65 ml), carbon disulfide (0.91 ml) and n-butyl iodide (3.3 g) are reacted and treated. The product is crystallized from chloroform to give the title compound (1.9 g) as pale yellow crystals, m.p. 163°-164° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04628057 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-eadd99cbbc9c4f758ed6387d76fa90a4 |
| Source note | uspto-grants-1986_12 |