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HRID 41344作成日:2026年10月24日

Thionyl Chloride → Laurolactam

https://huagongshe.com/ja/reaction/41344

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物Cyclododecanone, oximeHCID 136762—
触媒ZincchlorideHCID 3007855—
溶媒TolueneHCID 1140—
生成物LaurolactamHCID 1369098.8%

反応条件

温度100 °C

反応手順

Within a glove box, 0.033 g (0.17 mmol) of cyclododecanone oxime prepared in Reference Example 2 was dissolved in 0.400 g of a 5% by weight thionyl chloride (rearrangement catalyst)/toluene solution (0.020 g (0.17 mmol) as pure thionyl chloride), and the mixture was stirred using a magnetic stirrer at room temperature (25° C.) for 5 min, to conduct the pre-preparation of a rearrangement catalyst. After the pre-preparation, high performance liquid chromatography analysis indicated that cyclododecanone oxime had been consumed. Separately, within a glove box (under nitrogen atmosphere), in a flat-bottom flask equipped with a manifold, 3.285 g (16.64 mmol) of cyclododecanone oxime and 0.023 g (0.17 mmol) of zinc chloride were weighed and then 7.00 g of toluene was added, and the materials were dissolved by heating the mixture to 100° C. in an oil bath. To the zinc-chloride containing solution of cyclododecanone oxime in toluene, the reaction mixture which had been prepared in the pre-preparation using cyclododecanone oxime and thionyl chloride in 1:1 molar ratio was added, which then reacted for 60 min. The reaction solution was clear without turbidity, and gas chromatography analysis indicated that a conversion of cyclododecanone oxime was 100% and a laurolactam yield was 98.8%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530645B2
出典データセットuspto-grants-2013_09
ORD IDord-00b8032a959e4335b0845a1c12a5a3f9
出典メモuspto-grants-2013_09