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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLauric AcidHCID 3893—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant3-((Tert-butyldimethylsilyl)oxy)piperidineHCID 22352414—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1-oxododecyl-3-(O-tert-butyldimethylsilyoxy)piperidineHCID 18989546—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05489600
Source datasetuspto-grants-1996_02
ORD IDord-09da1355281f47208f3af32d81f56483
Source noteuspto-grants-1996_02