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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 551742생성일: 2026년 10월 26일

Water → 15-Hydroxypentadecanoic acid

https://huagongshe.com/reaction/551742

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriphenylphosphineHCID 11776—
반응물15-Hydroxypentadecanoic acidHCID 78360—
반응물2-methoxyethyl N-(2-methoxyethoxycarbonylimino)carbamateHCID 53384415—
용매TetrahydrofuranHCID 8028—
생성물15-Hydroxypentadecanoic acidHCID 78360—
생성물PentadecalactoneHCID 235414—

반응 단계

After triphenylphosphine (366 mg, 1.39 mmol) and THF (135 mL) were added to a 300 mL flask, azodicarboxylic acid bis(2-methoxyethyl) ester (367 mg, 1.39 mmol) dissolved in THF (30 mL) was added dropwise thereto at 20° C. Subsequently, 15-hydroxypentadecanoic acid (300 mg, 1.16 mmol) dissolved in THF (60 mL) was added dropwise thereto at 20° C., and the reaction was allowed to proceed for 12.5 hours. Water (0.5 mL) was added, and concentration was carried out. Then, water (15 ml) was added to the solution, and extraction was carried out using diethyl ether (15 ml, ×2). Then, the organic layer was washed with water (15 mL) and saturated salt water (15 ml), and dehumidified with anhydrous magnesium sulfate. Subsequently, a crude product obtained by concentration was purified by column chromatography (silica gel, 5% ethyl acetate-hexane solution) to give 15-pentadecanolactone as a white solid substance (86 mg, yield: 31%/15-hydroxypentadecanoic acid).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947816B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-e64fc7bd4cda4dfa9752d22794246d67
출처 메모uspto-grants-2011_05