HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65077Generated: October 29, 2026
Iodoethane → Ethyl (1RS, 3SR)-trans-1-ethyl-3-hydroxymethyl-1,2,3,4-tetrahydro-beta-carboline-2-carbodithioate
https://huagongshe.com/reaction/65077
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (1RS, 3SR)-trans-1-ethyl-3-hydroxymethyl-1,2,3,4-tetrahydro-beta-carboline | HCID 86741006 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Ethyl (1RS, 3SR)-trans-1-ethyl-3-hydroxymethyl-1,2,3,4-tetrahydro-beta-carboline-2-carbodithioate | HCID 86741017 | 71% |
Reaction Steps
(1RS, 3SR)-trans-1-Ethyl-3-hydroxymethyl-1,2,3,4-tetrahydro-β-carboline (0.461 g) is dissolved in dimethylsulfoxide (2 ml), and thereto are added CS2 (0.27 ml) and triethylamine (0.61 ml). The mixture is stirred at room temperature for one hour, and thereto is added dropwise ethyl iodide (0.38 ml), and the mixture is stirred at room temperature for 2 hours. The reaction mixture is poured onto ice-water, and the mixture is extracted with ethyl acetate. The extract is washed with water, dried over sodium sulfate and then distilled to remove the solvent. The residue is recrystallized from aqueous ethanol to give the title compound (0.477 g, 71%) as colorless needles, m.p. 82°-84° C., NMR (CDCl3, δ): 1.40 (t, J=7.0 Hz, 3H, CSSCH2CH3); Mass m/e: 334 (M+), 272 (M+ --CH3CH2SH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04612317 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-abb64ae05e0b47a79a5cdf6d6a9f60d8 |
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| Source note | uspto-grants-1986_09 |
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