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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1015458생성일: 2026년 10월 25일

Water → 4,4'-Oxybis(benzene-1,2-dimethanol)

https://huagongshe.com/reaction/1015458

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium HydroxideHCID 14798—
반응물4,4'-Oxydiphthalic anhydrideHCID 74574—
반응물Aluminium lithium hydrideHCID 21226445—
용매AcetoneHCID 180—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물4,4'-Oxybis(benzene-1,2-dimethanol)HCID 5977945998.7%

반응 단계

To a solution of LiAlH4 (1M in THF) (64 mL, 64.0 mmol, 4.0 molar equivalents) in THF (50 mL) cooled to −78° C. is added dropwise a solution of 4,4′-oxydiphthalic anhydride (5.0 g, 9.6 mmol, 1 molar equivalent) in THF (20 ml). The reaction mixture is allowed to warm up to room temperature and then stirred at 70° C. for 2 hrs. To this resulting solution cooled at 0° C. is added a 2M sodium hydroxide solution (40 mL) followed by cold water (25 mL) and THF (50 mL). The reaction mixture is then further extracted with THF (3×50 mL). The organic fractions are combined, washed with brine, dried as added over magnesium sulfate, filtered and concentrated in vacuum to give a light brown oil. The crude oil is dissolved in acetone and Et2O is added until an off-white precipitate started to form. After filtration, the organic layer is concentrated in vacuum to give a light brown oil which crystallises spontaneously. Purification by DCM washes gave the title compound as a light yellow powder (2.75 g, 59%). 1H NMR (300.13 MHz, DMSO-d6) (ppm) 4.47 (d, J=5.40 Hz, 4H) 4.53 (d, J=5.40 Hz, 4H) 5.03 (t, J=5.40 Hz, 2H) 5.12 (t, J=5.40 Hz, 2H) 6.84 (dd, J1=2.70 Hz, J2=8.40 Hz, 2H) 7.04 (d, J=2.70 Hz, 2H) 7.34 (d, J=8.40 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07985353B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-f9a05eaab0e94d1882bd54b12c0b85b6
출처 메모uspto-grants-2011_07