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HRID 1654983作成日:2026年10月27日

Methanol → 11-(2-Cyanoethyl)-1,4,8,11-tetraazacyclotetradecane

https://huagongshe.com/reaction/1654983

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物TolueneHCID 1140—
反応物Sodium HydroxideHCID 14798—
反応物1,4,8,11-TetraazacyclotetradecaneHCID 64964—
反応物Dimethylformamide dimethyl acetalHCID 78373—
溶媒WaterHCID 962—
生成物11-(2-Cyanoethyl)-1,4,8,11-tetraazacyclotetradecaneHCID 10515058—

反応手順

13.68 g (114.8 mmol) of dimethylformamide-dimethylacetal (under nitrogen) is added to 20.0 g (99.83 mmol) of 1,4,8,11-tetraazacyclotetradecane in 200 ml of absolute toluene. It is refluxed slowly and the solvent is distilled off in this way. Then, it is concentrated by evaporation under reduced pressure. The residue is cooled to room temperature. 6.36 g (119.8 mmol) of acrylic acid nitrile is instilled under a nitrogen atmosphere and heated slowly to 75° C. It is stirred for 9 hours at this temperature. It is cooled to room temperature and a mixture of 120 ml of methanol/30 ml of water is added. It is stirred for 10 minutes at room temperature. Then, 11.98 g (299.5 mmol) of sodium hydroxide is added and it is stirred for 24 hours at 40° C. It is evaporated to dryness in a vacuum and the residue is extracted 3 times with hot toluene (80° C.). The organic phase is dried on potassium hydroxide and concentrated by evaporation in a vacuum.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05410043
出典データセットuspto-grants-1995_04
ORD IDord-d9b9d30967e445fb9581ec7680003df2
出典メモuspto-grants-1995_04