関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tyrosine Methyl Ester | HCID 70652 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | O-(tert-butyldiphenylsilyl)-L-tyrosine methyl ester | HCID 53905505 | 87.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US06015887 |
|---|
| 出典データセット | uspto-grants-2000_01 |
|---|
| ORD ID | ord-87039577dfd94d8998a5be8198a65934 |
|---|
| 出典メモ | uspto-grants-2000_01 |
|---|