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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445898Generated: October 31, 2026

Sodium hydride → HCID 59170339, compound

https://huagongshe.com/reaction/1445898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-bromoisovalerateHCID 79068—
Reactant1-Benzyl-2-methyl-1H-indol-4-olHCID 10752360—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 59170339HCID 5917033919.5%

Reaction Steps

1-Benzyl-2-methyl-1H-indol-4-ol 3 (0.3 g 1.26 mmole) was dissolved in anhydrous dimethylformamide (20 mL). To the solution sodium hydride 60% in mineral oil (66 mg 1.65 mmole) was added. The mixture was stirred at room temperature for 1 h. To the mixture ethyl-2-bromoisovalerate (0.344 mL, 1.65 mmole) was added. The mixture was stirred at room temperature for 18 h. The reaction was diluted with ethyl acetate (300 mL) and washed with H2O (4×100 mL) and brine (1×100 mL). The organic layer was separated, dried with magnesium sulfate and concentrated. The residue was purified by column chromatography (10:1 Hexane:EtOAc) to afford a 1:1 mixture of 7: ethyl-2-bromoisovalerate. Further purification by column chromatography (10:1 Hexane:EtOAc) afforded 7 (0.09 g, 19%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666898B2
Source datasetuspto-grants-2010_02
ORD IDord-d1b980aff94e44e6886df00ea8b24b12
Source noteuspto-grants-2010_02