돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 965848생성일: 2026년 10월 26일

Iodine → 2-Chloro-6-(hydroxymethyl)-4-iodo-3-pyridinol

https://huagongshe.com/reaction/965848

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium BisulfateHCID 516919—
반응물2-Chloro-6-(hydroxymethyl)-3-pyridinolHCID 11423742—
용매WaterHCID 962—
생성물2-Chloro-6-(hydroxymethyl)-4-iodo-3-pyridinolHCID 1068456862.2%

반응 단계

2-Chloro-6-(hydroxymethyl)-3-pyridinol (11.6 g, 72.7 mmol) and NaHCO3 (18.3 g, 218 mmol) are dissolved in 200 ml water in a flask. The mixture is stirred until homogeneous, is cooled in an ice bath, is treated with iodine (19.4 g, 76.3 mmol), and is stirred over 60 h at rt as the cooling bath expired. The pH of the mixture is adjusted to 3 with 2N NaHSO4, and the mixture is extracted with 4×50 ml EtOAc. The combined organic layer is dried (MgSO4) and is concentrated in vacuo to a yellow solid. The crude solid is washed with EtOAc to provide 12.9 g (62%) of 2-chloro-6-(hydroxymethyl)-4-iodo-3-pyridinol as an off-white solid. The filtrate is concentrated to a small volume and is chromatographed over 250 g SiO2 (230-400 mesh) eluting with EtOAc/CH2Cl2/hexane/acetic acid 2.5:4.5:4:0.1. The appropriate fractions are combined and concentrated to afford an additional 2.4 g (12%) of pure 2-chloro-6-(hydroxymethyl)-4-iodo-3-pyridinol. MS for C6H5ClINO2, m/z: 285 (M)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06951868B2
출처 데이터셋uspto-grants-2005_10
ORD IDord-f8b9977570e745fda8dcc06868bd11cf
출처 메모uspto-grants-2005_10