돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83992생성일: 2026년 10월 23일

Iodine → phenylalaninol, (S)-

https://huagongshe.com/ko/reaction/83992

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물L-PhenylalanineHCID 6140—
반응물Potassium HydroxideHCID 14797—
반응물Sodium borohydrideHCID 4311764—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물phenylalaninol, (S)-HCID 447213118.4%

반응 조건

온도0 °C

반응 단계

To a suspension of sodium borohydride (16.5 g) in dry tetrahydrofuran (600 mL), (L)-phenylalanine (30 g) was added at one portion. The flask was cooled to 0° C. under nitrogen atmosphere. Iodine (46.18 g) solution in tetrahydrofuran (150 mL) was added slowly in drop-wise manner over 40 minutes, resulting in vigorous evolution of H2. After the complete addition of iodine, the reaction mixture was heated to reflux for 18 hours and cooled to room temperature. The reaction mixture was quenched with methanol until the reaction mixture became clear. Further, the solution was stirred for 30 minutes at room temperature. The solvents were removed by rotary evaporation to obtain a white paste which was dissolved by 20% aqueous potassium hydroxide (450 mL). The solution was stirred for 4 hours and then dichloromethane was added. The organic layers were separated and the aqueous layer was extracted with dichloromethane. The combined organic layers were washed with brine and dried over anhydrous sodium sulfate. The solvents were evaporated under reduced pressure to afford 32.5 g of (L)-phenylalaninol as a viscous liquid. The crude product was used as such for the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846910B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-65f4865e8b474b37b97982db917a5472
출처 메모uspto-grants-2014_09