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HRID 1069554作成日:2026年10月23日

Sodium hydride → HCID 53700123、化合物

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

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物4-Benzyloxybenzyl chlorideHCID 70042—
反応物Ethyl (5-methoxy-2-methyl-1H-indol-3-yl)acetateHCID 10729163—
反応物HCID 21191889HCID 21191889—
生成物HCID 53700123HCID 53700123—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06252084B1
出典データセットuspto-grants-2001_06
ORD IDord-480e139e4306421181e72a34f0e7b9b8
出典メモuspto-grants-2001_06