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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217783생성일: 2026년 10월 24일

Boron trifluoride etherate → 3-(4-Bromophenyl)propan-1-ol

https://huagongshe.com/ko/reaction/217783

반응식

참여 물질

역할이름HCID투입량
반응물Boron trifluoride etherateHCID 8000—
반응물TetrahydrofuranHCID 8028—
반응물3-(2-Bromophenyl)propionic acidHCID 316010—
반응물Sodium borohydrideHCID 4311764—
용매WaterHCID 962—
용매tert-Butyl methyl etherHCID 15413—
생성물3-(4-Bromophenyl)propan-1-olHCID 10560614—

반응 조건

온도25 °C

반응 단계

Sodium borohydride (119.12 g) and THF (5 L) were charged into reactor 1 and temperature adjusted to −20° C. 3-(bromophenyl)propionic acid (1 kg) was charged into reactor 2 with THF (3 L) and stirred at 25° C. until all the solids dissolved. This solution in reactor 2 was transferred to reactor 1 maintaining reactor 1 contents at <0° C. BF3.Et2O (991.4 g) was slowly added into reactor 1 maintaining reactor 1 contents at −20 to −10° C. After addition, the mixture was stirred at −20 to −10° C. for 1 h. The reaction is analysed for completion (3-(bromophenyl)propionic acid <2.5%). Water (2 L) was slowly added into reactor 1 to quench the reaction. (gas evolution). MTBE (5 L) was charged into reactor 1 and phases separation was carried out. The upper layer was collected and lower layer was washed with MTBE (5 L). The upper layer was collected and combined with the layer from the previous step. Adjusted pH value of the organic layer to 8-9 by adding 1N NaOH solution. The organic layer was washed with saturated NaCl solution (2 L) and the upper layer was collected. The organic layer was evaporated down to a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198285B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-34040895c7734d0f8dcdc8093bf0d886
출처 메모uspto-grants-2012_06