HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986253Generated: October 31, 2026
Oxalyl chloride → HCID 20158336, compound
https://huagongshe.com/reaction/986253
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 9(10H)-Acridinone, 10-(2-(diethylamino)ethyl)- | HCID 148883 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20158336 | HCID 20158336 | — |
Reaction Steps
A solution of 11.5 g of 10-[2-(diethylamino)ethyl]-9-acridanone in 250 ml of dichloromethane is treated at -5° and within 0.5 hour with 6.7 ml of oxalyl chloride, stirred at room temperature for 1 hour, the yellow crystals (9-chloro-10-[2-(diethylamino)ethyl]acridinium chloride) which have formed are filtered and washed successively with methylene chloride and petroleum ether. The material obtained is taken up in 200 ml of methanol, treated with 3.6 g of thiosemicarbazide and stirred at room temperature for about 18 hours. The precipitated salt is filtered and washed successively with ethanol and ether. There is obtained 10-[2-(diethylamino)ethyl]-9-acridanone thiosemicarbazone dihydrochloride (crystallizing with 1 mol of methanol) of melting point 124° (decomposition). This material is treated with 1N sodium hydroxide solution and extracted with dichloromethane. The solution is washed with water, dried and evaporated, whereupon the product is crystallized from acetonitrile. There is obtained 10-[2-(diethylamino)ethyl]-9-acridanone thiosemicarbazone of melting point 154°-156°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04711889 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-4fd62ed375404f83ae9f15a08ba58a95 |
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| Source note | uspto-grants-1987_12 |
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