HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369986Generated: October 28, 2026
Hydrochloric Acid → HCID 21584389, compound
https://huagongshe.com/reaction/369986
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | HCID 13150100 | HCID 13150100 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 21584389 | HCID 21584389 | 36% |
Reaction Steps
To a solution of 1,2,3,5,10,10a-hexahydropyrrolo[1,2-b]isoquinoline (4.12 g, 23.8 mmol) in concentrated sulfuric acid (100 ml) at -10° C. was added, in portions over 1 h, potassium nitrate (2.40 g, 23.7 mmol). After addition was complete, the reaction mixture was stirred for 1 h before it was poured over ice. The aqueous solution was made basic with concentrated ammonium hydroxide and the product was extracted into dichloromethane (twice). The dried (magnesium sulfate) organic phase was concentrated to give a red oil that solidified on standing. This solid was taken up in isopropanol (100 ml) and hydrogen chloride in ethanol was added until acidic. The solid was collected, washed with isopropanol and dried to give the crude product (3.39 g, 56%). This solid was recrystalized from ethanol to give the title compound (2.16 g, 36%) as an off-white solid, m.p. 231-3° C. (dec.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06140322 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-58de5e365fd742a4ba70a942b4c4f4d1 |
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| Source note | uspto-grants-2000_10 |
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