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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 73293생성일: 2026년 10월 24일

Diethanolamine → 2-Butyl-1,3,6,2-dioxazaborocane

https://huagongshe.com/ko/reaction/73293

반응식

참여 물질

역할이름HCID투입량
반응물DiethanolamineHCID 8113—
반응물Butylboronic AcidHCID 20479—
반응물2,3-Dihydroxy-N~1~,N~1~,N~4~,N~4~-tetramethylbutanediamideHCID 6999257—
반응물DioxazaborocinHCID 57497284—
용매DichloromethaneHCID 6344—
용매Sodium chloride; waterHCID 57417360—
생성물2-Butyl-1,3,6,2-dioxazaborocaneHCID 346607—

반응 단계

2-(But-1-yl)-tetrahydro-4H-1,3,6,2-dioxazaborocine [CAS 92527-13-4] was prepared from n-butylboronic acid and 2-(2-hydroxy-ethylamino)-ethanol [CAS 111-42-2] as reported in Organic Synthesis, 1998, 76, 86-96. This dioxazaborocine (3 g, 17.5 mmol) and (2S,3S)-2,3-dihydroxy-N,N,N′,N′-tetramethyl-butanediamide [CAS 63126-52-3] (4.65 g) were dissolved in anhydrous dichloromethane (95 mL) under N2. Brine (30 mL) was added. The resulting mixture was stirred at room temperature for 1 hour. The two layers were separated, and the aqueous layer was extracted with dichloromethane (30 mL). The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated in vacuo to provide the title compound as an oil 1H NMR (300 MHz, CDCl3): δ 0.82-0.9 (m, 5H), 1.25-1.45 (m, 4H), 2.98 (s, 6H), 3.2 (s, 6H), 5.52 (s, 2H). MS (DCl—NH3) m/z 271 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829041B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-d8d8b063e05b4152bcb42186af8a356e
출처 메모uspto-grants-2014_09