돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 907510생성일: 2026년 10월 25일

Pyridine → HCID 46945492, 화합물

https://huagongshe.com/reaction/907510

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Chlorosulfurous acid, ethyl esterHCID 80784—
반응물2,2-Bis(hexyloxy)propan-1-olHCID 46945302—
용매DichloromethaneHCID 6344—
생성물HCID 46945492HCID 4694549288%

반응 조건

온도23 °C

반응 단계

To a solution of alcohol 4 (20.6 g, 79.1 mmol) in CH2Cl2 (200 mL) is added pyridine (8.12 g, 102.8 mmol) and ethyl chlorosulfite (12.2 g, 94.9 mmol). The reaction mixture is stirred at 23° C. for 10 hours. The reaction is quenched with water (100 mL) and extracted with CH2Cl2 (2×100 mL). The combined organic layers are washed with HCl (1N, 100 mL), saturated NaHCO3 (100 mL), brine (100 mL) and dried over anhydrous sodium sulfate. The solvent is removed and the residue is purified by silica gel chromatography (1→10% ethyl acetate/hexane) to give 2,2-bis(hexyloxy)propanyl ethyl sulfite 6 (24.5 g, 88%) as a colorless oil: Rf (15% EtOAc/hexane)=0.44; IR (thin film, cm−1) 2932, 2872, 1467, 1379, 1213, 1194, 1176, 1001, 888; 1H NMR (600 MHz, CDCl3) δ 4.11-4.00 (m, 2H), 3.93 (d, J=10.8 Hz, 1H), 3.77 (d, J=10.8 Hz, 1H), 3.42-3.37 (m, 4H), 1.51-1.48 (m, 4H), 1.33 (s, 3H), 1.31-1.24 (m, 15H), 0.85 (t, J=7.2 Hz, 6H); 13C NMR (150 MHz, CDCl3) δ 99.0, 62.9, 60.8, 58.5, 58.3, 31.6, 29.8, 25.9, 22.6, 20.9, 15.3, 14.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08013179B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-269d6cbc819a42239a372bed210b9cb3
출처 메모uspto-grants-2011_09