HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491938Generated: October 27, 2026
Dodecanoyl chloride → 2,6-Diphenyl-4-piperidyl laurate
https://huagongshe.com/reaction/1491938
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dodecanoyl chloride | HCID 8166 | — |
| Reactant | 2,6-Diphenylpiperidin-4-ol | HCID 13068932 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2,6-Diphenyl-4-piperidyl laurate | HCID 15250484 | 74.2% |
Reaction Steps
To a -70° C. solution of 2.50 g (9.9 mmol) of 2,6-diphenyl-4-hydroxypiperidine in 80 ml of dry tetrahydrofuran (THF), 4.2 mL (10.5 mmol) of n-butyllithium (2.5M in hexanes) is added dropwise. The mixture is warmed to -20° C. and stirred for 30 minutes. The solution is then cooled again to -70° C. and a solution of 2.2 g (9.9 mmol) of lauroyl chloride in 20 mL of dry THF is then added dropwise. The mixture is warmed to room temperature and stirred for 18 hours. The mixture is added to 250 mL of brine and then extracted with 2×200 mL of ether. The combined organic layers are dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue is purified by liquid chromatography (LC) (silica gel, ethyl acetate/hexane) to give 3.2 g (74%) of the title compound as a white solid: mp 40°-42° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05371125 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-66a8b80031fa4934ba5e8b697152ca4b |
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| Source note | uspto-grants-1994_12 |
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