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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 270642생성일: 2026년 10월 26일

Trimethyl borate → 2-(3-Hydroxymethylthiophen-2-yl)ethanol

https://huagongshe.com/reaction/270642

반응식

참여 물질

역할이름HCID투입량
반응물Trimethyl borateHCID 8470—
반응물Lithium BromideHCID 82050—
반응물Methyl 2-(2-methoxy-2-oxoethyl)thiophene-3-carboxylateHCID 58952963—
반응물HCID 178418435HCID 178418435—
용매MethanolHCID 887—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물2-(3-Hydroxymethylthiophen-2-yl)ethanolHCID 1118276190.6%

반응 단계

To 800 mL of anhydrous tetrahydrofuran, 31.0 g of sodium boron hydride and 71.3 g of lithium bromide were added, and then 10.6 mL of trimethyl borate was added thereto dropwise at 0° C. The resulting mixture was stirred at room temperature for 30 minutes, and then a solution obtained by dissolving 70.4 g of the compound obtained in Example 1 in 200 mL of tetrahydrofuran was slowly added over 2 hours while allowing the resulting mixture to reflux. The reaction solution was further refluxed for 2 hours then cooled to room temperature. 100 mL of anhydrous methanol was added slowly to the solution, and then 700 mL of ethyl ether and 700 mL of water were added. The organic phase was collected, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to obtain 47.1 g (yield of 90%) of the title compound as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449580B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-da60a17647834b40847d67500597ec76
출처 메모uspto-grants-2008_11