HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446921Generated: October 27, 2026
Sodium hydride → 3,6-Bis(4-chlorobutoxy)acridine hydrochloride
https://huagongshe.com/reaction/1446921
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Chlorobutyl 4-methylbenzenesulfonate | HCID 12422128 | — |
| Reactant | Acridine-3,6-diol | HCID 135482596 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3,6-Bis(4-chlorobutoxy)acridine hydrochloride | HCID 20553471 | — |
Reaction Steps
To a mixture of 11.8 g. of sodium hydride (61.1% dispersion in oil) and 26.0 g. of 3,6-acridinediol is added 250 ml. of dimethylformamide. The mixture is stirred at room temperature for 1.5 hours, then 52.5 g. of 4-chlorobutyl-p-toluenesulfonate are added. This mixture is stirred at room temperature for 3 hours and 20 minutes and then at 50° C. for 2 hours. The volatile materials are removed under reduced pressure at 35°-40° C. The residue is quenched with 1200 ml. of ice-cold saturated aqueous sodium bicarbonate. The resulting tan crystals are collected and dissolved in 500 ml. of chloroform, 30 ml. of 6 N hydrochloric acid in isopropanol are added and the mixture is diluted with ether, giving the desired product as the hydrochloride salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04314061 |
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| Source dataset | uspto-grants-1982_02 |
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| ORD ID | ord-dd578601a4e14a4aa06a5b133593bd49 |
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| Source note | uspto-grants-1982_02 |
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