Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,6-Diethyl-2,3,6-trimethyl-1-(1-phenylethoxy)piperidin-4-ol | HCID 22341851 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21361327 | HCID 21361327 | — |
Reaction Steps
To a solution of 6.36 g (2 mmol) of 2,6-diethyl-2,3,6-trimethyl-1-(1-phenyl-ethoxy)-piperidin-4-ol (prepared as described in GB 2335190, example 7, compound 102) and 2.02 g (2 mmol) of triethylamine in 50 ml toluene are added 1.57 g (2 mmol) acetyl chloride at 0–5° C. and the reaction mixture is stirred for 2 hours at 20° C. The reaction mixture is then several times extracted with water. The organic phase is dried over Na2SO4 and after removing the solvent 6.9 g (96%) acetic acid 2,6-diethyl-2,3,6-trimethyl-1-(1-phenyl-ethoxy)-piperidin-4-yl ester are obtained as yellowish liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07160966B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-e0259b34a6564ddebaed8cb0a1c4b5b4 |
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| Source note | uspto-grants-2007_01 |
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