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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23237생성일: 2026년 10월 23일

Sodium Bromide → N-benzyl-N-(tert-butoxycarbonyl)-L-phenylalaninal

https://huagongshe.com/ko/reaction/23237

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BromideHCID 253881—
반응물Sodium BicarbonateHCID 516892—
반응물TempoHCID 2724126—
반응물N-(t-Butoxycarbonyl)-N-benzyl-L-phenylalaninolHCID 15434535—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물N-benzyl-N-(tert-butoxycarbonyl)-L-phenylalaninalHCID 11099858100.3%

반응 조건

온도0 °C

반응 단계

To a solution of 0.32 g (0.94 mmoles) of N-(t-Butoxycarbonyl)-N-benzyl-L-phenylalaninol from Example 17 in 2.8 mL of toluene was added 2.4 mg (0.015 mmoles) of 2,2,6,6-tetramethyl-1-piperidinyloxy, free radical (TEMPO), 0.1 g (0.97 mmoles) of sodium bromide, 2.8 mL of ethyl acetate and 0.34 mL of water. The mixture was cooled to 0° C. and an aqueous solution of 4.2 mL of 5% household bleach containing 0.23 g (3.0 mL, 2.738 mmoles) of sodium bicarbonate was added slowly over 30 minutes. The mixture was stirred at 0° C. for 10 minutes. Three more additions (0.4 mL each) of bleach was added followed by stirring for 10 minutes after each addition to consume all the stating material. The two phase mixture was allowed to separate. The aqueous layer was extracted twice with 8 mL of toluene. The combined organic layer was washed with 1.25 mL of a solution containing 0.075 g of potassium iodide, sodium bisulfate (0.125 g) and water (1.1 mL), 1.25 mL of 10% aqueous sodium thiosulfate solution, 1.25 mL of pH 7 phosphate buffer and 1.5 mL of brine solution. The organic solution was dried over magnesium sulfate, filtered and concentrated under reduced pressure to give 0.32 g (100% yield) of N-(t-Butoxycarbonyl)-N-benzyl-L-phenylalaninal.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06849760B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-cd584cd671de40ce934aa9b679127836
출처 메모uspto-grants-2005_02