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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345986Generated: October 26, 2026

Water → 2,4-Bis-butylamino-6-(2,2,6,6-tetramethyl-4-benzoylpiperidin-1-yl)-1,3,5-triazine

https://huagongshe.com/reaction/345986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantO-XyleneHCID 7237—
ReactantButylamineHCID 8007—
ReactantSodium HydroxideHCID 14798—
Reactant2,4-Dichloro-6-(2,2,6,6-tetramethyl-4-benzoyloxy-piperidin-1-yl)-1,3,5-triazineHCID 19991752—
Product2,4-Bis-butylamino-6-(2,2,6,6-tetramethyl-4-benzoylpiperidin-1-yl)-1,3,5-triazineHCID 57138297—

Reaction Steps

20.5 g of 2,4-dichloro-6-(2,2,6,6-tetramethyl-4-benzoyloxypiperidin-1-yl)-1,3,5-triazine (prepared according to Example 2) are stirred in 200 ml of xylene with 8.0 g of n-butylamine at reflux for 4 hours. 4.4 g of pulverized sodium hydroxide are added to the reaction mixture and it is stirred for a further 15 hours at reflux. The contents of the flask are cooled to room temperature and, after addition of 100 ml of water, are vigorously stirred until the precipitated salt has completely gone into solution. The aqueous phase is separated off, and the xylene solution is washed three times, each with 100 ml of water, and evaporated in vacuo. The oily residue is dried at 100° and 13 Pa. 2,4-Bis-butylamino-6-(2,2,6,6-tetramethyl-4-benzoylpiperidin-1-yl)-1,3,5-triazine is obtained as a yellowish viscous material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05059689
Source datasetuspto-grants-1991_10
ORD IDord-6ec7564c092242d599acd3e691bce00e
Source noteuspto-grants-1991_10