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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1463537생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1463537

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1-Hydroxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidineHCID 688178—
반응물Potassium cyanateHCID 11378442—
반응물HCID 178513472HCID 178513472—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물1-Carbamoyloxy-4-benzoyloxy-2,2,6,6-tetramethylpiperidineHCID 1909057681%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05300647
출처 데이터셋uspto-grants-1994_04
ORD IDord-fd3396c6288947c492ab1d4e064a036a
출처 메모uspto-grants-1994_04