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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34566Generated: October 26, 2026

Piperidin-2-ylmethanol → N-(3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenoyl)-2-hydroxymethylpiperidine

https://huagongshe.com/reaction/34566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidin-2-ylmethanolHCID 94263—
Reactant3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenic acidHCID 128570—
ProductN-(3,7,11,15-Tetramethyl-2,6,10,14-hexadecatetraenoyl)-2-hydroxymethylpiperidineHCID 5383159594%

Reaction Steps

The procedure of Example 1 was repeated except that 6.1 g of 3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenoic acid and 3.5 g of 2-hydroxymethylpiperidine were used as starting materials. 7.5 g (yield 94%) of the title compound was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04762829
Source datasetuspto-grants-1988_08
ORD IDord-93e161664f034de6b88afd36a2870e93
Source noteuspto-grants-1988_08