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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 429913생성일: 2026년 10월 23일

Sulfuric Acid → tert-butyl (2S)-2-amino-3-(4-hydroxy-3-iodophenyl)propanoate

https://huagongshe.com/ko/reaction/429913

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물IsobutyleneHCID 8255—
반응물3-Iodo-L-TyrosineHCID 439744—
반응물Sodium BicarbonateHCID 516892—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물tert-butyl (2S)-2-amino-3-(4-hydroxy-3-iodophenyl)propanoateHCID 5729194158%

반응 단계

A mixture of 5.0 g of 3-iodo-L-tyrosine (Aldrich) and 2.5 mL of conc. H2SO4 in 85 mL of 1,4-dioxane was added to 30 mL of liquid isobutylene (condensed at −78° C.) in a 300 mL pressure bottle. The vessel was stoppered and the contents stirred at RT. After 3 days the bottle was cooled in an ice water bath, opened and the solution poured into a mixture of 10 g of NaHCO3 in 150 mL of water. The resulting mixture was subjected to rotary evaporation to remove isobutylene and dioxane. A white solid resulted which was collected by filtration and dried in vacuo. Analysis by tlc (SiO2, 95:5 CH2Cl2:MeOH) indicated major and minor components at Rf=0.52 and 0.60 respectively. The crude product was purified by flash chromatography on silica gel (95:5 CH2Cl2:MeOH) to afford 3.4 g (58%) of tert-butyl 3-iodo-L-tyrosinate as a white crystalline solid, m.p. 158-159° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06319702B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-5fb542aab96648f592defa820e5599a9
출처 메모uspto-grants-2001_11