HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972221Generated: October 29, 2026
Dichloromethane → HCID 21399508, compound
https://huagongshe.com/reaction/972221
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21399514 | HCID 21399514 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21399508 | HCID 21399508 | — |
Reaction Steps
40 ml. of dichloromethane are added to a suspension of 1.00 g. of 1-ethyl-1-(2-cyanoethyl)-1,2,3,4,6,7-hexahydro-12H-indolo(2,3 -a)quinolizinium perchlorate in 100 ml. of distilled water, and the pH of the mixture is adjusted to 10 to 11 with 40% sodium hydroxide solution. During this operation the mixture is cooled with water and stirred in argon atmosphere. After some minutes of stirring the separated red organic phase is removed, and the aqueous phase is extracted with 20 ml. of dichloromethane. The organic solutions are combined, dried over magnesium sulfate, and the solvent is evaporated in vacuo. The obtained 0.75 g. of red, oily residue is triturated with 1 ml. of methanol, and the resulting orange-red crystals are filtered off. 0.72 g. of (1-ethyl-1,2,3,4,6,7-hexahydro-indolo[2,3-a]quinolizin-1-yl)-propionitrile are obtained; m.p.: 122-123° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04052404 |
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| Source dataset | uspto-grants-1977_10 |
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| ORD ID | ord-8fd0853bcfe042febd549581ba0a01fa |
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| Source note | uspto-grants-1977_10 |
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