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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 39205생성일: 2026년 10월 24일

Potassium Carbonate → Boc-serinol Bisphthalonitrile

https://huagongshe.com/ko/reaction/39205

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1,2-Benzenedicarbonitrile, 3-nitro-HCID 162652—
반응물N-Boc-serinolHCID 10631565—
용매BenzeneHCID 241—
용매Dimethyl SulfoxideHCID 679—
용매AcetonitrileHCID 6342—
생성물Boc-serinol BisphthalonitrileHCID 6897937570%

반응 단계

Finely ground K2CO3 (4.32 g, 31.2 mmol, 4 equiv.) was added to N-Boc-serinol (1.45 g, 7.8 mmol, 1 equiv.) in 20 mL DMSO under argon; then 3-nitrophthalonitrile (3.38 g, 19.5 mmol, 2.5 equiv.) was added. The reaction mixture first turned pink, and then orange upon addition of the 3-nitrophthalonitrile. The reaction mixture was stirred at room temperature and monitored periodically by TLC (9:1 benzene:CH3CN). After 72 h, the reaction mixture was partitioned between EtOAc and water. The two layers were separated, and the aqueous layer was extracted 3 times with 50 mL EtOAc. The organic layer from the original partitioning was added to the organic extract. This mixture was then washed twice with 50 mL of saturated NaHCO3, and twice with 50 mL of water, and was then dried over Na2SO4. The solvent was removed at reduced pressure, and the resulting crude orange solid was recrystallized from methanol/water to give 2.43 g (70% yield) of a slightly pink/tan solid. [Rf: 0.25 (9:1 benzene:CH3CN); melting point 167-169° C.; 1H NMR (200 MHz, CD3CN) δ 7.85-7.4 (m, 6H, ArH), 5.76 (br s, 1H, NH), 4.39 (s, 5H, (—CH2)2CH—), 1.42 (s, 9H, C(CH3)3).]

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524891B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-888d8fed8607485c8c9c1b84f18a0627
출처 메모uspto-grants-2013_09