HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076833Generated: October 27, 2026
Ammonia → 1-(2-(4-Isothiocyanatophenoxy)ethyl)pyrrolidine
https://huagongshe.com/reaction/1076833
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | 4-(2-(Pyrrolidin-1-yl)ethoxy)aniline | HCID 6493749 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(2-(4-Isothiocyanatophenoxy)ethyl)pyrrolidine | HCID 11846122 | — |
Reaction Steps
4-(2-Pyrrolidin-1-ylethoxy)aniline (17.3 g.) in ethanol (20 ml.) is added dropwise to a mixture of ethanol (55 ml.), carbon disulphide (10 ml.) and aqueous ammonia (density = 0.88, 20 ml.) at 0°C. After 2 hours the solid is collected and washed with acetone, m.p. 143° - 150°C. (dec.). This solid (23.6 g.), chloroform (114 ml.) and triethylamine (11.9 ml.) are stirred, and ethyl chloroformate (8.6 ml.) added with cooling so that the temperature remains below 0°C. After stirring for 30 minutes below 0°C. and 1 hour at 20°C., excess of 10% sodium hydroxide is added. The chloroform is separated, washed with water, dried and evaporated. The residue is dissolved in benzene and the solution filtered through alumina. The filtrate is evaporated and the residue distilled to give 4-(2-pyrrolidin-1-ylethoxy)phenyl isothiocyanate, b.p. 160° - 168°C./0.2 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03957999 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-e71717069173479e983c7ee1f0aaef0f |
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| Source note | uspto-grants-1976_05 |
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