HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 838924Generated: November 1, 2026
Hydrochloric Acid → 3-Chloro-N-(3-chloropropyl)-N-methylpropan-1-amine--hydrogen chloride (1/1)
https://huagongshe.com/reaction/838924
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3,3'-(Methylazanediyl)bis(propan-1-ol) | HCID 228352 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Chloro-N-(3-chloropropyl)-N-methylpropan-1-amine--hydrogen chloride (1/1) | HCID 12557533 | — |
Reaction Steps
A solution of about 60 grams of N,N-bis(3-hydroxypropyl)methylamine in 110 ml of chloroform is saturated, with cooling and stirring, with anhydrous hydrogen chloride gas. To the resulting two-phase liquid mixture is added, over a period of about 30 minutes at a temperature of 0-5° C., approximately 66 ml of thionyl chloride. The homogeneous solution thus obtained is allowed to stand at room temperature for a period of about 15 hours, the solution is then heated at reflux temperature for an additional two-hour period, and the chloroform is evaporated in vacuo from the light brown-colored reaction solution. The residual material is washed with ethanol, and is then crystallized from a mixture of 200 ml ethanol: 800 ml ether. The white crystalline product thus obtained is recovered by filtration, washed with three portions of ether, then with hexane, and dried in vacuo at 25° C. to give about 80 grams of N,N-bis(3-chloropropyl) methylamine hydrochloride; m.p. 86-88° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04093657 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-b4f378b0ae7c44f68f4a0290e52c0aa5 |
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| Source note | uspto-grants-1978_06 |
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