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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 850142생성일: 2026년 10월 25일

Tyrosine Methyl Ester → O-(tert-butyldiphenylsilyl)-L-tyrosine methyl ester

https://huagongshe.com/reaction/850142

반응식

참여 물질

역할이름HCID투입량
반응물Tyrosine Methyl EsterHCID 70652—
반응물DiisopropylethylamineHCID 81531—
반응물tert-ButyldiphenylchlorosilaneHCID 94078—
용매DichloromethaneHCID 6344—
생성물O-(tert-butyldiphenylsilyl)-L-tyrosine methyl esterHCID 5390550587.8%

반응 단계

To a solution of L-tyrosine methyl ester (Sigma Chemical Company) (10.0 g, 51.3 mmol) and diisopropylethylamine (25.9 g, 200.0 mmol) in CH2Cl2 (400 mL) was added t-butyldiphenylsilyl chloride (TBDPS-Cl; 35.2 g, 128.2 mmol) at 23° C. The resultant mixture was stirred at 23° C. for 14 hours. The crude reaction mixture was dried over (MgSO4) and concentrated in vacuo. The resultant residue was purified by silica gel flash column chromatography. The polarity of the eluting solvent mixture was adjusted according to the Rf value of the product. The eluted fractions were combined, dried over MgSO4, concentrated and dried to give 19.5 g (87.8% yield) of O-(tert-butyldiphenylsilyl)-L-tyrosine methyl ester as a colorless syrup. Rf (hexanes/ethyl acetate (AcOEt)/methanol (MeOH) 20:20:1)=0.38.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06015887
출처 데이터셋uspto-grants-2000_01
ORD IDord-87039577dfd94d8998a5be8198a65934
출처 메모uspto-grants-2000_01