HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Disulfide → 2-Thenyl (3R)-3-hydroxymethyl-1,2,3,4-tetrahydro-beta-carboline-2-carbodithioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(Chloromethyl)thiophene | HCID 69830 | — |
| Reactant | (3R)-3-hydroxymethyl-1,2,3,4-tetrahydro-beta-carboline | HCID 13375507 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Thenyl (3R)-3-hydroxymethyl-1,2,3,4-tetrahydro-beta-carboline-2-carbodithioate | HCID 13687660 | 45% |
Reaction Steps
In the same manner as described in Example 8 by using (3R)-3-hydroxymethyl-1,2,3,4-tetrahydro-β-carboline (2.02 g), 2N NaOH (12.5 ml), CS2 (1.9 g), 2-thenyl chloride (3.31 g) and 80% ethanol (50 ml), there is prepared the title compound (1.68 g, 45%) as white powder, [α]D20 -113.8° (c=1.0, methanol). NMR (CDCl3, δ): 4.83 (s, 2H, ##STR10## Mass m/e: 374 (M+), 244 (M+ -- ##STR11##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04612317 |
| Source dataset | uspto-grants-1986_09 |
| ORD ID | ord-e13be12b8bc84b9399e529e513337e68 |
| Source note | uspto-grants-1986_09 |