돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26328생성일: 2026년 10월 24일

Benzyl Bromide → Boc-Ala-Ala-OBzl

https://huagongshe.com/ko/reaction/26328

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Cesium carbonateHCID 10796—
반응물N-((1,1-Dimethylethoxy)carbonyl)-L-alanyl-L-alanineHCID 6992569—
용매MethanolHCID 887—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Boc-Ala-Ala-OBzlHCID 10904242—

반응 단계

Boc-Ala-Ala-OH (7.23 g, 27.8 mmol) was dissolved in a mixture of 200 ml MeOH and 20 ml H2O.Cs2CO3 solution (20% aqueous) was added until the pH reached 7.0 (~30 ml) and the resultant neutral solution evaporated to dryness. The residue was re-evaporated twice with DMF (150 ml) and the gelatenous solid that remained was stirred in 120 ml DMF with benzyl bromide (7.2 g, 42 mmol) for 15 hours. The solvent was then removed by evaporation and the residue treated with 500 ml water. The product precipitated as an oil which gradually solidified on standing. It was taken up in EtOAc (400 ml), washed with H2O (3 times), dried (Na2SO4), and evaporated to a syrup which on treatment with petroleum ether began to crystallize. The product was recrystallized from EtOAc and petroleum ether to yield, 7.2 g (73.8%); mp 71°-73° (lit. mp 73°-74°; D. A. Laufer et al., J. Amer. Chem. Soc., 90, 2696 (1968)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04148788
출처 데이터셋uspto-grants-1979_04
ORD IDord-81d95717c968480c8febb41b4c95e2df
출처 메모uspto-grants-1979_04