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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 965459생성일: 2026년 10월 25일

Butyl iodide → 2',3'-Di-n-butoxy-2,6-dichloro-4'-methoxy-6'-methyl-benzophenone

https://huagongshe.com/reaction/965459

반응식

참여 물질

역할이름HCID투입량
반응물Butyl iodideHCID 10962—
반응물Sodium hydrideHCID 24758—
반응물2,6-Dichloro-2',3'-dihydroxy-4'-methoxy-6'-methyl-benzophenoneHCID 54569551—
용매TetrahydrofuranHCID 8028—
생성물2',3'-Di-n-butoxy-2,6-dichloro-4'-methoxy-6'-methyl-benzophenoneHCID 53713925—

반응 조건

온도100 °C

반응 단계

Sodiumhydride (0.4 g; 60%; 10 mmol) is added with stirring to a solution of 2,6-dichloro-2',3'-dihydroxy-4'-methoxy-6'-methyl-benzophenone (1.64 g; 5 mmol) in tetrahydrofurane. The solvent is evaporated and the residue dissolved in 30 ml of dimethylformamide. 1-iodo-n-butane (4.6 g; 25 mmol) is added, the mixture is stirred at 100° C. for 8 hours and then the solvent is evaporated. The residue is shaken with toluene/2N hydrochloric acid, the organic layer separated, washed with water and the solvent evaporated. The residue is purified by chromatography (flash column filled with 35 g of silicagel; elution with 500 ml of petrolether containing 2% of ethylacetate); yellow oil (0.7 g; 32% y).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05773663
출처 데이터셋uspto-grants-1998_06
ORD IDord-1c3f43f7342345d3bbb71eabe79c1ab1
출처 메모uspto-grants-1998_06