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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405300Generated: November 2, 2026

Lithium Hydroxide → 2-[4-Methoxy-3-(3-methyl-benzyloxymethyl)-benzoylamino]-indane-2-carboxylic acid

https://huagongshe.com/reaction/2405300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
Reactantm-Xylyl bromideHCID 12099—
ReactantSodium hydrideHCID 24758—
ReactantHCID 67076690HCID 67076690—
SolventDimethylformamideHCID 6228—
Solvent1,4-DioxaneHCID 31275—
Product2-[4-Methoxy-3-(3-methyl-benzyloxymethyl)-benzoylamino]-indane-2-carboxylic acidHCID 670767878%

Reaction Conditions

Temperature60 °C

Reaction Steps

The compound of step 2 (50 mg, 0.14 mmol)) was dissolved in DMF (3 ml) and sodium hydride (60% dispersion in mineral oil, 6.2 mg, 0.15 mmol) was added followed by 1-bromomethyl-3-methyl-benzene (27 mg, 0.14 mmol). The mixture was stirred overnight. Then lithium hydroxide (1 M solution in water, 0.42 ml) and dioxane (1 ml) were added and the mixture heated to 60° C. for 1 h. The residue was partitioned between 2 N hydrochloric acid and EA and the aqueous phase was extracted with EA. The combined organic phases were dried over sodium sulfate and evaporated to dryness. The residue was purified by RP HPLC (water/ACN gradient) to yield 5 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802720B2
Source datasetuspto-grants-2014_08
ORD IDord-7dadeecf80854e8fadf05d73cb5e50ae
Source noteuspto-grants-2014_08