HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658986Generated: October 30, 2026
Sodium Iodide → 2-[Ethyl(methyl)amino]propan-1-ol
https://huagongshe.com/reaction/658986
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | N-Methylethylamine | HCID 12219 | — |
| Reactant | 3-Chloro-1-propanol | HCID 12313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 3-[Ethyl(methyl)amino]propan-1-ol | HCID 14440969 | — |
| Product | 2-[Ethyl(methyl)amino]propan-1-ol | HCID 45791167 | 63.5% |
Reaction Steps
3-(N-ethyl-N-methylamino)propanol was prepared as follows: In a pressure vessel was mixed N-ethyl-N-methylamine (25 g, 420 mmol), 3-chloropropanol (14.1 mL, 16 g, 170 mmol), sodium iodide (2.54 g, 17 mmol) and 60 mL dioxane. The vessel was sealed and heated to 65° C. After 3 days the reaction was allowed to cool to ambient temperature. Solvent was removed by rotary evaporation leaving a brown oil. The oil was dissolved in 80 mL of 2N NaOH, extracted with EtOAc (3×250 mL) and dried over Na2SO4. After filtration of the drying agent solvent was removed in vacuo leaving a brown oil. The oil was distilled (75° C., 15 mm Hg) leaving 2-(N-ethyl-N-methylamino)propanol (6.3 g, 54 mmol, 32% yield) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08080548B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-efaa476288e444508c30097de62094dd |
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| Source note | uspto-grants-2011_12 |
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