HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309686Generated: October 31, 2026
Sodium hydride → 3,6-Bis(3-chloropropoxy)acridine--hydrogen chloride (1/1)
https://huagongshe.com/reaction/2309686
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Chloropropyl p-toluenesulfonate | HCID 69434 | — |
| Reactant | HCID 137195957 | HCID 137195957 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3,6-Bis(3-chloropropoxy)acridine--hydrogen chloride (1/1) | HCID 20184663 | — |
Reaction Steps
To a mixture of 11.80 g. of sodium hydride (61.14% oil dispersion) and 26.0 g. of 3,6-acridinediol sulfate (2:1) is added 250 ml. of dry N,N-dimethylformamide. The mixture is stirred at room temperature for 1.5 hours, then 49.8 g. of 3-chloropropyl-p-toluene sulfonate are added. This mixture is stirred at room temperature for 3 hours and 20 minutes, then at 50° C. for 2 hours. The volatile materials are removed under reduced pressure at 35°-40° C. and the residue is quenched with 1200 ml. of ice-cold saturated aqueous sodium bicarbonate solution. The resulting tan crystals are collected and dissolved in 500 ml. of chloroform. A 30 ml. portion of 6N hydrochloric acid in isopropanol is added and the mixture is diluted with ether. The solid is collected and recrystallized from ether, giving the desired product as tan crystals, m.p. 211°-213° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04696935 |
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| Source dataset | uspto-grants-1987_09 |
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| ORD ID | ord-02adb90c7d3f4611aac160147200240d |
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| Source note | uspto-grants-1987_09 |
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