Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl but-2-ynoate | HCID 141019 | — |
| Reactant | 2,6-Diethyl-2,3,6-trimethylpiperidin-4-ol | HCID 22182241 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 70604950 | HCID 70604950 | 76% |
Reaction Steps
To a solution of 3.0 g of 2,6-diethyl-2,3,6-trimethyl-4-piperidinol (Compound 1) in 30 ml of benzene was added, in small portions at room temperature, 0.72 g of 50 % sodium hydride. The mixture was then stirred for 30 minutes at room temperature. A solution of 2.2 g of methyl tetrolate in 10 ml of benzene was then added dropwise, with ice-cooling to the mixture and the whole mixture was stirred at room temperature for 64 hours. The mixture was then poured into ice water and extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride and then dried over anhydrous sodium sulphate. After removing the solvent, the residue was distilled under reduced pressure, giving 3.4 g of Compound 97 as a pale yellow oil (bp 109° - 111° C/0.15 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04075165 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-f5591fb2d3f74dceb82970607b1b9164 |
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| Source note | uspto-grants-1978_02 |
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