돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 347870생성일: 2026년 10월 27일

Iodine → 2,6-Dimethoxy-4-methoxymethylphenylboric acid

https://huagongshe.com/reaction/347870

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Trimethyl borateHCID 8470—
반응물Ammonium ChlorideHCID 25517—
반응물MagnesiumHCID 5462224—
반응물2-Bromo-1,3-dimethoxy-5-(methoxymethyl)benzeneHCID 23080940—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물2,6-Dimethoxy-4-methoxymethylphenylboric acidHCID 2308094589%

반응 조건

온도70 °C

반응 단계

To a suspension of magnesium turnings (97.5 mg, 4.01 mmol) in tetrahydrofuran (0.5 mL) containing a small amount of added iodine, was added approximately a tenth part of a solution of 2-bromo-1,3-dimethoxy-5-(methoxymethyl)benzene (1.0 g, 3.82 mmol) in tetrahydrofuran (1 mL) under a nitrogen atmosphere, and the mixture was heated in an oil bath at 70° C. The heating was terminated upon gentle reflux of the reaction mixture and fading of the iodine color. To continue the reflux, the remaining solution of 2-bromo-1,3-dimethoxy-5-(methoxymethyl)benzene in tetrahydrofuran was added dropwise to the reaction mixture. Upon completion of the dropwise addition, the reaction mixture was further heated to reflux for 1 hour and then cooled to room temperature. The reaction mixture was then added dropwise to an ice-cooled solution of trimethyl borate (0.57 mL, 4.97 mmol) in tetrahydrofuran (0.5 mL). Upon completion of the dropwise addition and stirring for 40 minutes while cooling with ice, the mixture was stirred overnight at room temperature. An aqueous ammonium chloride solution and methanol were then added to the reaction mixture. Quantitation by liquid chromatography confirmed that the title compound had been obtained at an 89% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07176216B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-b54b18ef27434a6ea3cb26a03f88f82d
출처 메모uspto-grants-2007_02