HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395713Generated: October 29, 2026
Lauric Acid → 1-oxododecyl-3-(O-tert-butyldimethylsilyoxy)piperidine
https://huagongshe.com/reaction/2395713
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lauric Acid | HCID 3893 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-((Tert-butyldimethylsilyl)oxy)piperidine | HCID 22352414 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-oxododecyl-3-(O-tert-butyldimethylsilyoxy)piperidine | HCID 18989546 | — |
Reaction Steps
Dissolve lauric acid (0.77 g) in methylene chloride (50mL) and cool to 0° C. Add oxalyl chloride (0.37 mL) and dimethylformamide (3 drops). Allow to warm to room temperature and stir for 1 hour. Add, by dropwise addition, to a solution of 3-(O-tert-butyldimethylsilyloxy)piperidine (0.76 g, 3.5 mmol) and triethylamine (1 mL) in methylene chloride (20 mL). Stir overnight. Dilute with methylene chloride (50 mL) and separate the organic phase. Wash twice with 10% sodium hydroxide, once with 10% hydrochloric acid, and once with saturated sodium hydrogen carbonate and once with brine. Dry (Na2SO4) and evaporate the solvent in vacuo to give 1-oxododecyl-3-(O-tert-butyldimethylsilyoxy)piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05489600 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-09da1355281f47208f3af32d81f56483 |
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| Source note | uspto-grants-1996_02 |
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