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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3364생성일: 2026년 10월 25일

Sodium hydride → (1-Benzyl-2-ethyl-1H-indol-4-yloxy)-acetic acid methyl ester

https://huagongshe.com/reaction/3364

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Methyl bromoacetateHCID 60984—
반응물1-Benzyl-2-ethyl-1H-indol-4-OLHCID 9816416—
생성물(1-Benzyl-2-ethyl-1H-indol-4-yloxy)-acetic acid methyl esterHCID 1068737169%

반응 단계

Using the procedure described in Example 1, Part E, 2-ethyl-4-hydroxy-1-(phenylmethyl)-1H-indole (1.56 g, 6.2 mmol) was treated with 248 mg (6.2 mmol) of 60% NaH/mineral oil and then 0.6 mL (6.2 mmol) of methyl bromoacetate. The product was purified by chromatography over silica gel eluting with 20% EtOAc/hexane, to give 1.37 g (69% yield) of [[2-ethyl-1-(phenylmethyl)-1H-indol-4-yl]oxy]acetic acid methyl ester, 89°-92° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733923
출처 데이터셋uspto-grants-1998_03
ORD IDord-093410cd99d04309ae041c581fea5247
출처 메모uspto-grants-1998_03