HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113250Generated: October 30, 2026
Sodium Methoxide → 7,7-Dimethyl-3-oxa-6-azaoctan-1-ol
https://huagongshe.com/reaction/2113250
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 86616350 | HCID 86616350 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7,7-Dimethyl-3-oxa-6-azaoctan-1-ol | HCID 13643664 | 70% |
Reaction Steps
2-(2-t-Butylaminoethoxy)ethyl acetate (1.2 g, 5.9 mmol) was stirred for 7 hours with sodium methoxide (0.015 g, 0.28 mmol) in methanol (15 mL) at room temperature. The NMR analysis of the reaction mixture showed approximately 20% conversion. Additional sodium methoxide (0.015 g, 0.28 mmol) was added to the reaction mixture and it was stirred for an additional 3 hours. Solvent was evaporated and the liquid phase was separated from the solid by filtration. The solid was washed with diethyl ether. The combined filtrates were evaporated under reduced pressure to remove a solvent to give 2-(2-t-butylamino-ethoxy)ethanol (EETB) as yellowish liquid (0.65 g, 70%) 1H NMR δ 1.12 (s, 9H), 2.76 (t, J=5.1 Hz, 2H), 3.59-3.66 (m, 4H), 3.70-3.73 (m, 2H); 13C NMR δ 28.8, 42.2, 50.3, 61.8, 71.3, 72.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524990B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-b2516ed036e64fc8b0f7e24a627f238f |
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| Source note | uspto-grants-2009_04 |
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