HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1115Generated: October 26, 2026
Nitrogen → 16-[N,N-bis(2-hydroxyethyl)amino]-1-hexadecanol
https://huagongshe.com/reaction/1115
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N,N-bis(2-hydroxyethyl)-16-hydroxyhexadecanamide | HCID 19694613 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 16-[N,N-bis(2-hydroxyethyl)amino]-1-hexadecanol | HCID 22015146 | 62% |
Reaction Steps
A 500-ml flask equipped with a stirrer and reflux condenser was charged with 3.01 g (79.3 mmol) of LiAlH4 and 200 ml of tetrahydrofuran. While stirring the mixture at room temperature in an N2 atmosphere, 5.00 g (13.9 mmol) of N,N-bis(2-hydroxyethyl)-16-hydroxyhexadecanamide were added, followed by stirring at 65° C. for 18 hours. After cooling the reaction mixture to room temperature, 15 g of 3% aqueous KOH were added, and a salt deposited was separated by filtration. The solvent was then distilled off under reduced pressure, and the resultant residue was purified by column chromatography on silica gel, thereby obtaining 2.98 g (yield: 62%) of the title compound (IId-3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05723497 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-f7c05078e24046a8887d238bff8b0c4f |
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| Source note | uspto-grants-1998_03 |
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