HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35067Generated: October 25, 2026
Carbon Disulfide → [3-[3-(1-Piperidinylmethyl)phenoxy]propyl]isothiocyanate
https://huagongshe.com/reaction/35067
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(1-Piperidinylmethyl)phenoxy propanamine | HCID 21297576 | — |
| Catalyst | Mercuric Chloride | HCID 24085 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | [3-[3-(1-Piperidinylmethyl)phenoxy]propyl]isothiocyanate | HCID 13391620 | — |
Reaction Steps
A solution of carbon disulphide (3.3 ml) in acetone (8 ml) was added dropwise to a solution of 3-[3-(1-piperidinylmethyl)phenoxy propanamine (12.4 g) in acetone (30 ml) over a 15 minute period, between -5° and -10° C. The solution was cooled to -14° C. and mercury (II) chloride (13.6 g) in acetone (30 ml) was added, during 45 minutes. Triethylamine (16 ml) was added at 0° C. during 15 minutes, and the mixture was heated at reflux for 45 minutes. The resulting suspension was purified by filtration and the filtrate evaporated in vacuo. The residue was purified by column chromatography using methanol as eluant to give the title compound (6 g) as an amber oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04764612 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-c5fa03e0c1ec46999ab8fa5c993f6693 |
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| Source note | uspto-grants-1988_08 |
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