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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069554Generated: October 23, 2026

Sodium hydride → HCID 53700123, compound

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-Benzyloxybenzyl chlorideHCID 70042—
ReactantEthyl (5-methoxy-2-methyl-1H-indol-3-yl)acetateHCID 10729163—
ReactantHCID 21191889HCID 21191889—
ProductHCID 53700123HCID 53700123—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06252084B1
Source datasetuspto-grants-2001_06
ORD IDord-480e139e4306421181e72a34f0e7b9b8
Source noteuspto-grants-2001_06