HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446910Generated: October 31, 2026
Sodium hydride → 3,6-Bis(3-chloropropoxy)acridine--hydrogen chloride (1/1)
https://huagongshe.com/reaction/1446910
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 6 N 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 | US04314061 |
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| Source dataset | uspto-grants-1982_02 |
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| ORD ID | ord-cb58491186eb4580bfa5540fcf032c0c |
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| Source note | uspto-grants-1982_02 |
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