Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637261Generated: October 30, 2026

Water → 1-Methoxycarbonylmethyl-2-phenyl-1,3,4,5-tetrahydrobenz[cd]indol-5-one

https://huagongshe.com/reaction/1637261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantMethyl bromoacetateHCID 60984—
Reactant2-Phenyl-1,3,4,5-tetrahydrobenz[cd]indol-5-oneHCID 19348368—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-Methoxycarbonylmethyl-2-phenyl-1,3,4,5-tetrahydrobenz[cd]indol-5-oneHCID 1934832190%

Reaction Steps

A solution of the compound (1.37 g) obtained in Example 41 in anhydrous dimethylformamide (DMF; 60 ml) was added to a suspension of sodium hydride (60% dispersion in oil; 0.30 g) in DMF(10 ml) at room temperature. After stirring for 15 minutes, a solution of methyl bromoacetate (0.72 ml) in DMF (10 ml) was added to the reaction mixture. The reaction mixture was stirred for 10 minutes at room temperature, followed by addition of water and extraction with three portions of ethyl acetate. The organic layer was washed with water and saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the residue was crystallized from ethyl acetate to yield 1.58 g (90%) of the titled compound as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06040331
Source datasetuspto-grants-2000_03
ORD IDord-56236f5626df490288eac5b1ef260539
Source noteuspto-grants-2000_03