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HRID 596874作成日:2026年10月26日

Hydrochloric Acid → 4-Ethyl-2-(p-methoxybenzyl)-1,3,3-trimethyl-4-piperidinol hydrochloride

https://huagongshe.com/reaction/596874

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物2-PiperidoneHCID 12665—
反応物Sodium HydroxideHCID 14798—
反応物1-HydroxypiperidineHCID 20935—
反応物2-[(4-Methoxyphenyl)methyl]-1,3,3-trimethylpiperidin-4-oneHCID 16726139—
反応物HCID 178506846HCID 178506846—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物4-Ethyl-2-(p-methoxybenzyl)-1,3,3-trimethyl-4-piperidinol hydrochlorideHCID 2144861645%

反応手順

The hydrochloride (18 g) of 2-(p-methoxybenzyl)-1,3,3-trimethyl-4-piperidone is converted to the free base by shaking with ether and aqueous sodium hydroxide, followed by evaporation of the ethereal solution. The oily base is dissolved in 30 ml of absolute ether and subsequently reacted with ethyl lithium (3.6 g in 300 ml of benzene) under conditions as described in example 39. According to gaschromatographic examination, conversion to the piperidinol occurs to the extent of only 25 percent. After the addition of water the reaction mixture is worked up as described in example 39 and the crude mixture of piperidone and piperidonal so obtained is treated again with ethyl lithium (2.7 g in 250 ml of benzene). This procedure is repeated once more whereafter still 20 percent of the piperidone appears to be present. Processing as usually furnishes 19 g of an oily base, which is converted to the hydrochloride with the aid of ethanolic hydrogen chloride. After the addition of acetone and ether, 9 g of the above crystalline product separates. Yield 45%. Melting point 232 -234° C with decomposition.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04012392
出典データセットuspto-grants-1977_03
ORD IDord-ae190895684a4db69ca756c37cf010e0
出典メモuspto-grants-1977_03