돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 323702생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/323702

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, in EP Publication No. 0 675 110, 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]oxyl]acetic acid methyl ester; mp 89-92° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06214855B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-9b76f4e8300747e7a5f0afc07b641bf8
출처 메모uspto-grants-2001_04