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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1069554생성일: 2026년 10월 24일

Sodium hydride → HCID 53700123, 화합물

https://huagongshe.com/ko/reaction/1069554

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물4-Benzyloxybenzyl chlorideHCID 70042—
반응물Ethyl (5-methoxy-2-methyl-1H-indol-3-yl)acetateHCID 10729163—
반응물HCID 21191889HCID 21191889—
생성물HCID 53700123HCID 53700123—

반응 단계

1-[(4-Benzyloxyphenyl)methyl]-5-methoxy-2-methyl-1H-indole-3-acetic acid. Using the method described in Example 6, Part A, 2.0 g (8.12 mmol) of 5-methoxy-2-methyl-1H-indole-3-acetic acid ethyl ester, 0.325 g (8.12 mmol) of 60% NaH/mineral oil, and 1.88 g (8.12 mmol) of 4-benzyloxy-1-chloromethylbenzene were reacted to give on workup 800 mg of crude 1-[(4-benzyloxyphenyl)methyl]-5-methoxy-2-methyl-1H-indole-3-acetic acid ethyl ester. The crude ester in 50 mL of MeOH and 15 mL of 1N NaOH was heated at reflux temperature for 3 hours and left standing for 16 hours. After diluting with water, the mixture was made acidic with 1N HCl and extracted with EtOAc. The EtOAc solution was dried (Na2SO4) and concentrated. The residue was crystallized from MeOH to give 280 mg (32% yield) of 1-[(4-benzyloxyphenyl)-methyl]-5-methoxy-2-methyl-1H-indole-3-acetic acid, mp, 175-179° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06252084B1
출처 데이터셋uspto-grants-2001_06
ORD IDord-480e139e4306421181e72a34f0e7b9b8
출처 메모uspto-grants-2001_06