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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1060428생성일: 2026년 10월 26일

Potassium Carbonate → N-(tert-butoxycarbonyl)-3,4-bis(2,6-dichlorobenzyloxy)-L-phenylalanine methyl ester

https://huagongshe.com/reaction/1060428

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2,6-Dichlorobenzyl chlorideHCID 74832—
반응물(S)-Methyl 2-((tert-butoxycarbonyl)amino)-3-(3,4-dihydroxyphenyl)propanoateHCID 14889488—
촉매Tetrabutylammonium IodideHCID 67553—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-(tert-butoxycarbonyl)-3,4-bis(2,6-dichlorobenzyloxy)-L-phenylalanine methyl esterHCID 5453025571.8%

반응 단계

2,6-Dichlorobenzyl chloride (1.73 g) was added to a suspension of N-(tert-butoxycarbonyl)-3,4-dihydroxy-L-phenylalanine methyl ester (2.5 g), K2CO3 (2.22 g), and n-Bu4NI (0.297 g) in DMF (15 mL) at room temperature. The mixture was stirred overnight at room temperature, diluted with water and extracted with ether. The extract was dried (MgSO4) and evaporated. The residue was purified by column chromatography (silica gel; eluent: hexanes/CH2Cl2/EtOAc, 5:5:1) to yield N-(tert-butoxycarbonyl)-3,4-bis(2,6-dichlorobenzyloxy)-L-phenylalanine methyl ester (2.0 g), ESMS: m/z 630 (MH+), N-(tert-butoxycarbonyl)-3-(2,6-dichlorobenzyloxy) -4-hydroxy-L-phenylalanine methyl ester (0.39 g), ESMS: m/z 470 (MH+), and N-(tert-butoxycarbonyl)-4-(2,6-dichlorobenzyloxy)-3-hydroxy-L-phenylalanine methyl ester (0.45 g), ESMS: m/z 470 (MH+), respectively.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06521666B1
출처 데이터셋uspto-grants-2003_02
ORD IDord-5a4d1d64491645f8951bcf4cfd31dc5c
출처 메모uspto-grants-2003_02