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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 574128생성일: 2026년 10월 24일

Tetrahydrofuran → 3-Hydroxymethyl-beta-carboline

https://huagongshe.com/ko/reaction/574128

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Methyl 9H-pyrido(3,4-b)indole-3-carboxylateHCID 107704—
반응물Sodium borohydrideHCID 4311764—
용매WaterHCID 962—
생성물3-Hydroxymethyl-beta-carbolineHCID 5353338—

반응 단계

3-carbomethoxy-β-carboline or a derivative thereof (J in Scheme VII above) is dissolved in a polar solvent (e.g., THF), and a reducing agent (e.g., NaBH4) is added to the solution. The mixture is stirred for a few hours and cooled. An excess of water is then added, and the mixture is stirred for another few hours. The solvent is thereafter evaporated and the resulting residue is dissolved in water, washed several times with one or more non-polar solvents such as dichloromethane and ethyl acetate, and the combined organic extracts are then evaporated. The remaining residue is purified by column chromatography (e.g., on a silica gel with elution by a 9:1 mixture of ethylacetate and methanol), to give a 3-hydroxymethyl-β-carboline intermediate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09034872B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-ec33a9ffa6874c778560b7e2fa43f17d
출처 메모uspto-grants-2015_05