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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1433309생성일: 2026년 10월 27일

1-(Chloromethyl)-2-iodobenzene → (3-Formyl-4-(2-iodo-benzyloxy)-phenyl)-acetic acid methyl ester

https://huagongshe.com/reaction/1433309

반응식

참여 물질

역할이름HCID투입량
반응물1-(Chloromethyl)-2-iodobenzeneHCID 101064—
반응물2-NaphthylalanineHCID 185915—
반응물Methyl 2-(3-formyl-4-hydroxyphenyl)acetateHCID 12374099—
용매TolueneHCID 1140—
용매AcetonitrileHCID 6342—
생성물(3-Formyl-4-(2-iodo-benzyloxy)-phenyl)-acetic acid methyl esterHCID 11682982—

반응 단계

A solution of (3-formyl-4-hydroxy-phenyl)-acetic acid methyl ester (17.2 g, 85.9 mmol) in acetonitrile was slowly added to a solution of 1-chloromethyl-2-iodo-benzene (13.06 g, 94.5 mmol) and Nal (3.22 g, 21.5 mmol) in acetonitrile (273 ml) at reflux temperature and the mixture was mantained at this temperature for 3 hours. Once the mixture reached room temperature, the residue that had formed was filtered, washed with acetonitrile and concentrated to obtain a residue that was then dissolved in toluene (330 ml) and washed with NaOH 0.1N and water. The organic layer was concentrated to dryness, diluted with acetone (330 ml) and was stirred into water (500 ml) at room temperature. The mixture was filtered and washed with water to obtain 33.959 (96%) of [3-Formyl-4-(2-iodo-benzyloxy)-phenyl]-acetic acid methyl ester, which was purified by crystallization in toluene-cyclohexane (99% HPLC)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07612219B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-6cdb77fceeb14b63b7ac2bc4f30fd8f5
출처 메모uspto-grants-2009_11