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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1518171생성일: 2026년 10월 26일

Pyridine → HCID 46945492, 화합물

https://huagongshe.com/reaction/1518171

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참여 물질

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

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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, 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 번호US08232423B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-a8cdb0dfb99f47739419e5360d136d5d
출처 메모uspto-grants-2012_07