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HRID 39205作成日:2026年10月24日

Potassium Carbonate → Boc-serinol Bisphthalonitrile

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

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1,2-Benzenedicarbonitrile, 3-nitro-HCID 162652—
反応物N-Boc-serinolHCID 10631565—
溶媒BenzeneHCID 241—
溶媒Dimethyl SulfoxideHCID 679—
溶媒AcetonitrileHCID 6342—
生成物Boc-serinol BisphthalonitrileHCID 6897937570%

反応手順

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).]

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524891B2
出典データセットuspto-grants-2013_09
ORD IDord-888d8fed8607485c8c9c1b84f18a0627
出典メモuspto-grants-2013_09