HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977162Generated: October 30, 2026
Sodium Hydroxide → HCID 11823533, compound
https://huagongshe.com/reaction/977162
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 15294370 | HCID 15294370 | — |
| Reactant | Sodium bis(2-methoxyethoxy)aluminiumhydride | HCID 21584525 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 11823533 | HCID 11823533 | 64% |
Reaction Steps
10 ml of bis(2-methoxyethoxy)aluminium-sodium hydride was added dropwise to a solution of 2.95 g (8.7×10-2 mole) of 1-dodecyl-α,α-dimethyl-4-piperidine-acetamide in 80 ml of methylbenzene. After stirring for one hour at room temperature, the mixture was refluxed for three hours. After cooling the mixture, 50 ml of 3N sodium hydroxide was carefully added and stirring was continued for 24 hours. The resulting mixture was extracted with methylbenzene. The organic phase was washed with water, dried over magnesium sulphate and filtered and the solvents were evaporated off under reduced pressure. The product was purified using silica gel chromatography, eluting with a 4/1/0.1 (v/v/v) ethyl acetate/methanol/ammonia mixture. 1.8 g (yield: 64%) of 1-dodecyl-β,β-dimethyl-4-piperidineethanamine was obtained as an oil. The (E)-2-butenedioate was obtained from this oil in an acetone-ether mixture. M Pt=100°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05614534 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-3a0f8577c45f448da55bcece375501a4 |
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| Source note | uspto-grants-1997_03 |
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