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HRID 1463537作成日:2026年10月27日

Hydrochloric Acid → 1-Carbamoyloxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidine

https://huagongshe.com/reaction/1463537

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1-Hydroxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidineHCID 688178—
反応物Potassium cyanateHCID 11378442—
反応物HCID 178513472HCID 178513472—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物1-Carbamoyloxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidineHCID 1909057681%

反応手順

A solution of 6.7 ml of 12 N HCl in 10 ml of water is added dropwise over 10 minutes with cooling below 0° C. to a suspension of 20.8 g (75 mmol) of 1-hydroxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidine, 75 ml of methanol, and 25 ml of water in a nitrogen atmosphere. A clear solution resulted. A solution of 6.1 g (75 mmol) of potassium cyanate in 25 ml of water is added dropwise over 30 minutes. The reaction temperature is maintained at 0-5° C. during the cyanate addition. The reaction mixture is stirred 30 minutes at ambient temperature, then filtered. The precipitate is washed with water, then dissolved in 200 ml of toluene. Residual water is removed by azeotropic distillation. The toluene solution is then cooled to yield 19.4 g (81%) of a white crystalline solid, m.p. 148-49° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05300647
出典データセットuspto-grants-1994_04
ORD IDord-fd3396c6288947c492ab1d4e064a036a
出典メモuspto-grants-1994_04