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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1173041생성일: 2026년 10월 26일

[4-Methyl-2-(phenyloxy)-1,3-thiazol-5-yl]methanol → 4-Methyl-2-(phenyloxy)-1,3-thiazole-5-carbaldehyde

https://huagongshe.com/reaction/1173041

반응식

참여 물질

역할이름HCID투입량
반응물[4-Methyl-2-(phenyloxy)-1,3-thiazol-5-yl]methanolHCID 57665456—
촉매Manganese dioxideHCID 14801—
용매ChloroformHCID 6212—
생성물4-Methyl-2-(phenyloxy)-1,3-thiazole-5-carbaldehydeHCID 5766548680%

반응 단계

A mixture of [4-methyl-2-(phenyloxy)-1,3-thiazol-5-yl]methanol (X-3a) (0.109 g, 0.492 mmol) and MnO2 (0.22 g, 2.56 mmol) in chloroform (2.5 mL) was stirred at RT for 2 h. More MnO2 was added (0.22 g) and continued to stir overnight. Additional MnO2 was added (0.40 g), and the mixture stirred for 3 days. The mixture was filtered through a pad of Celite, and the Celite was washed with EtOAc. The filtrate was concentrated, and the crude material was purified by chromatography (EtOAc/hexanes) to give the title compound as a colorless oil (0.086 g, 80%). 1H NMR (400 MHz, CDCl3) δ 9.93 (s, 1H), 7.46 (t, J=8.0 Hz, 2H), 7.33 (t, J=7.4 Hz, 1H), 7.29-7.27 (m, 2H), 2.60 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07834013B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-9ebb8632ab3742e6a6fc912442aa732c
출처 메모uspto-grants-2010_11