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HRID 218121作成日:2026年10月25日

L-Serine → N-Oleoyl-L-Serine

https://huagongshe.com/reaction/218121

反応式

関与物質

役割名称HCID仕込み量
反応物L-SerineHCID 5951—
反応物Oleic AcidHCID 445639—
反応物Sodium BicarbonateHCID 516892—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物N-Oleoyl-L-SerineHCID 44190514—

反応手順

A solution of hydroxysuccinimide ester of oleic acid (395 mg, 1 mmole) in tetrahydrofuran (10 ml) was added to a solution of L-serine (105 mg, 1 mmole) and sodium bicarbonate 84 mg, 1 mmole) in water (10 ml). The reaction mixture was let stirring overnight at room temperature, evaporated down to 10 ml, and acidified to pH 1 with 1 N HCl. The product was extracted with methylene chloride (2×20 mL) and dried (MgSO4) and the solvent evaporated under reduced pressure. The crude material was chromatographed on silica gel (eluting with chloroform:methanol) to give 221.7 mg (60%) as a white powder, m.p. 118 C, NMR (CD3OH, ppm): 5.35-5.32 (m, 2H), 4.57-4.36 (m, 1H), 3.90-3.85 (dd, J=12 Hz, 6 Hz, 1H), 3.82-3.78 (dd, J=12Hz, 6 Hz, 1H), 2.29-2.24 (t, 2H), 2.03-1.98 m, 4H), 1.68-1.58 (m, 2H), 1.32-1.29 (m, 22H), 0.91-0.87 (t, 3H). GC-MS (dTMS): 513, 498, 250, 132 m/z; LC-MS(−p): (M-H)+=368 m/z.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198327B2
出典データセットuspto-grants-2012_06
ORD IDord-f7a2089e17d24e64bf1bbfd3495da5c8
出典メモuspto-grants-2012_06