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HRID 850142作成日:2026年10月26日

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

https://huagongshe.com/reaction/850142

反応式

関与物質

役割名称HCID仕込み量
反応物Tyrosine Methyl EsterHCID 70652—
反応物DiisopropylethylamineHCID 81531—
反応物tert-ButyldiphenylchlorosilaneHCID 94078—
溶媒DichloromethaneHCID 6344—
生成物O-(tert-butyldiphenylsilyl)-L-tyrosine methyl esterHCID 5390550587.8%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06015887
出典データセットuspto-grants-2000_01
ORD IDord-87039577dfd94d8998a5be8198a65934
出典メモuspto-grants-2000_01