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HRID 2071929作成日:2026年10月24日

Sebacoyl chloride → Bis(1,2,2,6,6-pentamethyl-4-piperidyl) sebacate

https://huagongshe.com/ja/reaction/2071929

反応式

関与物質

役割名称HCID仕込み量
反応物Sebacoyl chlorideHCID 66072—
反応物4-Piperidinol, 1,2,2,6,6-pentamethyl-HCID 75472—
反応物1,2,2,6,6-Pentamethylpiperidin-4-ol hydrochlorideHCID 20492522—
溶媒BenzeneHCID 241—
生成物Bis(1,2,2,6,6-pentamethyl-4-piperidyl) sebacateHCID 586744—

反応手順

A solution of 17.10 parts of 1,2,2,6,6-pentamethylpiperidin-4-ol in 50 parts of dry benzene was stirred at 15°-20° C. whilst adding 6.0 parts of sebacoyl chloride dropwise over 15 minutes. The mixture was stirred for a further 12 hours at room temperature after which the 1,2,2,6,6-pentamethylpiperidin-4-ol hydrochloride formed during the reaction was filtered off. The benzene was removed by distillation under reduced pressure to give a yellow oil, which was distilled under reduced pressure to give bis(1,2,2,6,6-pentamethyl-4-piperidinyl)sebacate as a colorless oil having a boiling point of 218°-20° C. at 0.4 mm of Hg and the following elemental analysis by weight:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04049647
出典データセットuspto-grants-1977_09
ORD IDord-d6a1f4ccd52d4c7ab93b0288f2581946
出典メモuspto-grants-1977_09