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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1691063생성일: 2026년 10월 26일

Acetic Acid → (4-(5-Chloro-furan-2-ylmethyl)-phenyl)-methanol

https://huagongshe.com/reaction/1691063

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Potassium CarbonateHCID 11430—
반응물Sodium NitriteHCID 23668193—
반응물4-(5-Chloro-furan-2-ylmethyl)-benzylamineHCID 59255397—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물(4-(5-Chloro-furan-2-ylmethyl)-phenyl)-methanolHCID 5925537044%

반응 단계

To a mixture of 4-(5-chloro-furan-2-ylmethyl)-benzylamine (2.6 g) described in Manufacturing Example 62-1-2, acetic acid (25 mL) and water (25 mL) was added sodium nitrite (9.8 g, 140 mmol) at 0° C., which was stirred for 40 minutes at room temperature. Water and ethyl acetate were added to extract the reaction mixture. The organic layer was washed successively with water, saturated sodium hydrogencarbonate and saturated aqueous sodium chloride, and the solvent was evaporated under a reduced pressure. Methanol (25 mL) was added to the residue at 0° C., followed by addition of potassium carbonate (3.3 g, 24 mmol) at the same temperature. This was stirred for 1 hour at the same temperature. Water and ethyl acetate were added to extract the reaction mixture. The organic layer was washed successively with water, saturated sodium hydrogencarbonate and saturated aqueous sodium chloride, and the organic layer was concentrated under a reduced pressure. The residue was purified by neutral silica gel column chromatography (ethyl acetate:heptane=1:2) to obtain the title compound (1.2 mg, 44%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08153662B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-55743fa28a34413fab3dd88ffcf588fc
출처 메모uspto-grants-2012_04