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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2117009생성일: 2026년 10월 26일

p-Toluenesulfonic acid → L-Tyrosine

https://huagongshe.com/reaction/2117009

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물Cesium carbonateHCID 10796—
반응물Methyl bromoacetateHCID 60984—
반응물DiisopropylethylamineHCID 81531—
반응물Di-tert-butyl dicarbonateHCID 90495—
반응물(S)-Benzyl 2-amino-3-(4-hydroxyphenyl)propanoateHCID 104541—
용매TetrahydrofuranHCID 8028—
생성물L-TyrosineHCID 6057—

반응 단계

The para-toluenesulfonic acid salt of tyrosine benzyl ester (5.05 g, 11.4 mmol) was dissolved in THF (50 mL) containing DIEA (2.18 mL, 12.5 mmol) and di-tert-butyidicarbonate (2.98 g, 13.7 mmol) was added in one portion. The reaction was stirred 1.5 h at room temperature. Volatiles were removed under reduced pressure and the residue was dissolved in Et2O (150 mL). The solution was washed successively with water (25 mL), 5% citric acid (25 mL) and 5% NaHCO3 (25 mL). After drying (MgSO4), the solvent was evaporated under reduced pressure and the residue dissolved in acetone (100 mL). Cesium carbonate (4.83 g, 14.8 mmol) and methyl bromoacetate (1.3 mL, 13.7 mmol) were added and the heterogeneous mixture was stirred overnight at room temperature. Solids were then removed by filtration (acetone for washings) and the filtrate evaporated. The residue was dissolved in Et2O (150 mL) and washed with water (25 mL) and brine (25 mL). After drying (MgSO4), the solution was concentrated and the residue purified by flash chromatography using 25-50% EtOAc/hexane as eluent. The fully protected tyrosine derivative was obtained as a colorless oil (3.61 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07439258B2
출처 데이터셋uspto-grants-2008_10
ORD IDord-18db573d8e324bb38d3060ded58b676d
출처 메모uspto-grants-2008_10