HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580698Generated: October 29, 2026
Ammonium Chloride → 1-Acridinol, 1,2,3,4-tetrahydro-9-(methylamino)-
https://huagongshe.com/reaction/580698
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 13756050 | HCID 13756050 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 1-Acridinol, 1,2,3,4-tetrahydro-9-(methylamino)- | HCID 3025632 | 73% |
Reaction Steps
In 50 ml of dry tetrahydrofuran was dissolved 8.00 g of 3,4-dihydro-9-(methylamino)acridin-1(2H)-one. The mechanically stirred solution was cooled to -10° C. under N2 and 32 ml (1 eq) of 1.1M LiAlH4 solution in ether was added over 5 minutes. The stirring was continued for 45 minutes after the addition, during which the reaction went to completion. The excess LiAlH4 was neutralized with 1 ml of saturated NH4Cl and the resulting salts dissolved in 30% potassium hydroxide solution. The tetrahydrofuran solution was separated and evaporated to an oil which solidified upon trituration with 1:1 dichloromethane/hexanes. The solid was recrystallized from 10:1 hexanes/tetrahydrofuran to yield 5.89 g (73%) of a solid, melting point 160°-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04754050 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-173363e6092d4e09b0e26a35a3bc4aaa |
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| Source note | uspto-grants-1988_06 |
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