돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1637773생성일: 2026년 10월 27일

Allyl bromide → 2-Chloro-3-(1-propen-3-yl)-4-iodo-6-(1-hydroxyethyl)-pyridine

https://huagongshe.com/reaction/1637773

반응식

참여 물질

역할이름HCID투입량
반응물Allyl bromideHCID 7841—
반응물Ethyl AcetateHCID 8857—
반응물Sodium hydrideHCID 24758—
반응물2-Chloro-3-hydroxy-4-iodo-6-(1-hydroxyethyl)-pyridineHCID 10709299—
용매DimethylformamideHCID 6228—
생성물2-Chloro-3-(1-propen-3-yl)-4-iodo-6-(1-hydroxyethyl)-pyridineHCID 1879982093%

반응 단계

A solution of 2-chloro-3-hydroxy-4-iodo-6-(1-hydroxyethyl)-pyridine (3.6 g, 12 mmol) in 24 mL of N,N-dimethylformamide at 0° C. is treated with 480 mg (60% in oil, 12 mmol) of sodium hydride and stirred at room temperature for 1 h. The reaction is treated with 1.14 g (13.2 mmol) of allyl bromide and stirred for 2 h. The mixture is poured into 125 mL of ethyl acetate and washed with 4×50 mL of saturated sodium chloride, 2×25 mL of 50% saturated sodium carbonate and dried over potassium carbonate. The dried organics are concentrated in vacuo, diluted with 20 mL of hexanes, and chilled to -15° C. The solid is filtered to provide 3.61 g (89%) of 2-chloro-3-(1-propen-3-yl)-4-iodo-6-(1-hydroxyethyl)-pyridine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06043248
출처 데이터셋uspto-grants-2000_03
ORD IDord-1504d4b10e5840bea0191d477c57db87
출처 메모uspto-grants-2000_03