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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 548648생성일: 2026년 10월 23일

Citric Acid → 3-[((1S)-2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-1-methylethyl)oxy]-5-[(phenylmethyl)oxy]benzoic acid

https://huagongshe.com/ko/reaction/548648

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물WaterHCID 962—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물Methyl 3-((s)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-5-[(phenylmethyl)oxy]benzoateHCID 59127165—
용매TetrahydrofuranHCID 8028—
생성물3-[((1S)-2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-1-methylethyl)oxy]-5-[(phenylmethyl)oxy]benzoic acidHCID 5362963488.7%

반응 조건

온도45 °C

반응 단계

Methyl 3-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-5-[(phenylmethyl)oxy]benzoate (3.0 g, 6.98 mmol) was dissolved in THF (50 mL) and water (10 mL) and lithium hydroxide monohydrate (586 mg, 13.95 mmol) added. The resultant mixture was heated with stirring at 45° C. for 2 hours, then at ambient temperature for 16 hours, and at 45° C. for a further 4 hours. Water (40 mL) was added and the solvent removed in vacuo. The resultant solution was acidified carefully with 1M citric acid (2 equivalents), washed with water and brine then dried (MgSO4), filtered and evaporated in vacuo to give the title compound as a colourless gum (2.58 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07943607B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-53255cda81cf4972872396b3a3987613
출처 메모uspto-grants-2011_05