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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1372754생성일: 2026년 10월 25일

Iodo benzene diacetate → HCID 86592801, 화합물

https://huagongshe.com/reaction/1372754

반응식

참여 물질

역할이름HCID투입량
반응물Iodo benzene diacetateHCID 12217721—
반응물5-chloro-1-methyl-1H-indole-3-carbaldehydeHCID 16723796—
반응물Methyl 2-(4-amino-3-hydroxyphenyl)acetateHCID 17858854—
용매EthanolHCID 702—
생성물HCID 86592801HCID 8659280160.7%

반응 단계

In EtOH (9.0 ml), 5-chloro-1-methylindole-3-carbaldehyde (534 mg, 2.76 mmol) and methyl 4-amino-3-hydroxyphenylacetate (500 mg, 2.76 mmol) were stirred for hours. After iodobenzene diacetate (2.03 g, 6.31 mmol) was added to the reaction mixture and the mixture was stirred at room temperature for 1 hour, the solvent was distilled off under reduced pressure. The residue was purified by chromatography on a silica gel column, whereby from n-hexane-ethyl acetate (1:1, v/v) eluate fractions, a mixture (594 mg) of methyl (2-(5-chloro-1-methyl-3-indolyl)-6-benzoxazolyl)acetate and 5-chloro-1-methylindole-3-carboxaldehyde was obtained. To the resulting mixture were added THF (17 ml) and 0.25N NaOH (10.0 ml, 2.50 mmol) and the mixture was stirred at room temperature for 23 hours. The reaction mixture was distilled under reduced pressure to remove the solvent. To the residue was added 1N HCl (10 ml), followed by extraction with chloroform-methanol (4:1, v/v). The extract was dried over anhydrous sodium sulfate and distilled under reduced pressure to remove the solvent to give (2-(5-chloro-1-methyl-3-indolyl)-6-benzoxazolyl)acetic acid (88 mg, 9%) as a brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07157487B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-e5f5fdeeee46411ba4299e10dba6301f
출처 메모uspto-grants-2007_01