HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369961Generated: October 30, 2026
Hydrochloric Acid → 2-Hydroxyethyl-7-nitro-1,2,3,4-tetrahydroisoquinoline hydrochloride
https://huagongshe.com/reaction/369961
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 7-Nitro-1,2,3,4-tetrahydroisoquinoline hydrochloride | HCID 13521670 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Hydroxyethyl-7-nitro-1,2,3,4-tetrahydroisoquinoline hydrochloride | HCID 21584278 | 62% |
Reaction Steps
To a solution of 7-nitro-1,2,3,4-tetrahydroisoquinoline hydrochloride (5.01 g, 23.3 mmol) in ethanol (200 ml) at 0° C. in a pressure bottle was added 2.5 M sodium hydroxide solution (10 ml). This solution was stirred for 0.2 h before ethylene oxide (4.2 ml) was added and the bottle was capped and the solution was stirred overnight while slowly allowing it to warm to ambient temperature. The solvent was concentrated and the aqueous solution was extracted twice with dichloromethane. The combined and dried (magnesium sulfate) extracts were concentrated to give an oil. This oil was immediately dissolved in ethanol (125 ml) and hydrochloric acid in ethanol was added until a distinctly acidic solution was obtained. After cooling, the title compound was collected and isolated as an off-white solid (3.76 g, 62%), m.p. 213° 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-73a83ae02d634baa96960dccd5aa2e44 |
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| Source note | uspto-grants-2000_10 |
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