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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527002Generated: November 4, 2026

Benzoyl chloride → HCID 89739132, compound

https://huagongshe.com/reaction/1527002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium hydrideHCID 24758—
ReactantHCID 80156864HCID 80156864—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89739132HCID 8973913288%

Reaction Steps

To a suspension of sodium hydride (73 mg, w/w=60%, 1.8 mmol) tert-butyl 2-methyl-1H-indole-3-carboxylate (350 mg, 1.5 mmol) in tetrahydrofuran (30 mL) was added benzoyl chloride (250 mg, 1.8 mmol). The reaction solution was stirred at room temperature for 12 hours. The mixture was concentrated to give a residue, which was purified by column chromatography (silica gel, petroleum ether/ethyl acetate=3:1) to give tert-butyl 1-benzoyl-2-methyl-1H-indole-3-carboxylate (440 mg, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085583B2
Source datasetuspto-grants-2015_07
ORD IDord-03bdb811d531426ca4ef2bd705a4a20e
Source noteuspto-grants-2015_07