HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648106Generated: October 31, 2026
HCID 15917481, compound → HCID 15917483, compound
https://huagongshe.com/reaction/648106
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 15917481 | HCID 15917481 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15917483 | HCID 15917483 | — |
Reaction Steps
To a refluxing suspension of lithium aluminum hydride (1.4 g) in tetrahydrofuran (100 ml) is slowly dropped 6-chloro-2'-propionylspiro[benzofuran-2(3H),4'(2'H)-isoquinoline] (6.1 g) in tetrahydrofuran (50 ml). The reaction mixture is heated under reflux for four hours, cooled and quenched by the dropwise addition of saturated ammonium chloride solution (100 ml). The mixture is filtered, diluted with ether, washed with water (2X), saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After filtering, the solvent is removed to yield an oil which is dissolved in ether and converted to the product hydrochloride salt (6.0 g, 90%). The salt is recrystallized from ethyl acetate/methanol to yield the analytical sample as a white solid, mp 227°-228° (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04410699 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-2dc777c7b227440ea6ae6bc4923529bc |
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| Source note | uspto-grants-1983_10 |
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