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HRID 1900224作成日:2026年10月25日

1,4-Dihydroxy-2,2,6,6-tetramethylpiperidine → Bis(1-hydroxy-2,2,6,6-tetramethyl-4-piperidinyl)decandioate

https://huagongshe.com/reaction/1900224

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-Dihydroxy-2,2,6,6-tetramethylpiperidineHCID 5395—
反応物Dimethyl sebacateHCID 7829—
溶媒HeptaneHCID 8900—
生成物Bis(1-hydroxy-2,2,6,6-tetramethyl-4-piperidinyl)decandioateHCID 11272241—

反応条件

温度75 °C

反応手順

To a 300 ml three-necked flask fitted with a stirrer, nitrogen inlet, thermometer, condenser and Dean-Stark trap is added 34.45 g (0.2 mol) of 1-oxyl-2,2,6,6-tetramethylpiperidin-4-ol, 23.0 g (0.1 mol) of dimethyl sebacate and 110 ml of heptane. The reaction mixture is heated to reflux to dry the contents of the flask and 15 ml of slightly turbid distillate is removed from the Dean-Stark trap. The mixture is cooled to about 75° C. and 0.5 g of tetraisopropyl orthotitanate and 15 ml of heptane is added to the flask. The mixture is heated to reflux and heating at reflux temperature 100°-105° C. is continued for 24 hours with methanol being collected in the Dean-Stark trap. Water (5 ml) is added and heating is continued till all or most of the water is removed. The reaction mixture is allowed to cool slightly, is filtered and washed with heptane. Orange crystals form on standing and are collected by filtration, and washed with heptane. The orange crystalline product melts at 99°-101° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05574163
出典データセットuspto-grants-1996_11
ORD IDord-61e026dbcd3e4313ab2abb92ead260c6
出典メモuspto-grants-1996_11