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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25654생성일: 2026년 10월 25일

Sodium Thiosulfate → Benzyl methyl4-oxocyclohexylcarbamate

https://huagongshe.com/reaction/25654

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ThiosulfateHCID 24477—
반응물Potassium BromideHCID 253877—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium HypochloriteHCID 23665760—
반응물HCID 178485997HCID 178485997—
촉매TempoHCID 2724126—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물Benzyl methyl4-oxocyclohexylcarbamateHCID 5856280299%

반응 단계

A solution of 2.63 g (10 mmol) of cis-(4-Hydroxy-cyclohexyl)-methyl-carbamic acid benzyl ester in 16 ml CH2Cl2 was treated with a solution 0.24 g (2 mmol) of KBr and 0.28 g (3.33 mmol) of NaHCO3 in 5 ml of water. The suspension was cooled (0-5° C.) and 8 mg (0.05 mmol) of TEMPO and then 5.7 ml (12.5 mmol) of NaOCl (13%, 2.18 M in water) were added during 20 min. After 1 h at this temperature, again 8 mg (0.05 mmol) of TEMPO and then 2.85 ml (6.25 mmol) of NaOCl (13%, 2.18 M in water) were added. After 1 h, 5 ml of 1M sodium thiosulfat solution was added. The aqueous phase was extracted with CH2Cl2(2×), the organic phase was dried (Na2SO4), filtered and evaporated to give 2.57 g (99%) of Methyl-(4-oxo-cyclohexyl)-carbamic acid benzyl ester, MS: 261 (M).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858651B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-684046808ff74118b5c422a3a65be5d6
출처 메모uspto-grants-2005_02