戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 58364作成日:2026年10月26日

Potassium Carbonate → (S)-3-(4-But-3-enyloxy-phenyl)-2-tert-butoxycarbonylamino-propionic acid methyl ester

https://huagongshe.com/reaction/58364

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Homoallyl bromideHCID 21241—
反応物Boc-Tyr-OMeHCID 7019130—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物(S)-3-(4-But-3-enyloxy-phenyl)-2-tert-butoxycarbonylamino-propionic acid methyl esterHCID 66846982—

反応手順

N-BOC-tyrosine methyl ester (10.0 g, 33.9 mmol) was dissolved in DMF (40 mL) and potassium carbonate (5.62 g, 40.7 mmol) and 4-bromo-1-butene (4.13 mL, 40.7 mmol) were added. The mixture was stirred at rt for 18 h before being diluted with EtOAc (120 mL) and partitioned with 1M hydrochloric acid. The organic phase was washed with hydrochloric acid and then with brine before being dried (MgSO4), filtered and concentrated in vacuo. The crude material was purified by flash chromatography on silica using a gradient of EtOAc and (50/70) petroleum ether to yield a white solid, 3.20 g, 27%. Rf=0.82 (1/2 EtOAc/(50/70) petroleum ether).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434762B2
出典データセットuspto-grants-2016_09
ORD IDord-53224240deee4475a371d6a18ca920cc
出典メモuspto-grants-2016_09