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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971813Generated: October 28, 2026

Benzoyl chloride → HCID 21313377, compound

https://huagongshe.com/reaction/971813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantCalcium CarbonateHCID 10112—
ReactantSodium hydrideHCID 24758—
ReactantThionyl bromideHCID 68176—
Reactant(4-Methoxyphenyl)hydrazineHCID 77023—
ReactantEthyl 2-oxovalerateHCID 123521—
ReactantSodiumHCID 5360545—
ReactantHCID 11447063HCID 11447063—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 21313402HCID 21313402—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21313377HCID 21313377—

Reaction Steps

Reaction of 4-methoxyphenylhydrazine with ethyl α-ketovalerate in ethanol using the procedure described above in Example 1; reduction with lithium aluminum hydride in tetrahydrofuran of the resulting ethyl α-(5-methoxy-2-methyl-3-indole)acetate; reaction of the resulting 3-(2-hydroxyethyl)-5-methoxy-2-methylindole with sodium hydride in DMF, and reaction of the resulting sodium salt with benzoyl chloride using the procedure described above in Example 1; and reaction of the resulting 1-benzoyl-3-(2-hydroxyethyl)-5-methoxy-2-methylindole with thionyl bromide in benzene in the presence of calcium carbonate using the procedure described in U.S. Pat. No. 3,517,028 affords 1-benzoyl-3-(2-bromoethyl)-5-methoxy-2-methylindole. The latter, on reaction with an appropriate amine in refluxing acetone in the presence of sodium carbonate affords the compounds of formula I in Examples 72-77 below where, in each instance, R1 is 5-CH3O; R2 is CH3 ; A is C6H5CO; and Alk is CH2CH2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04160862
Source datasetuspto-grants-1979_07
ORD IDord-a1028e1e6ec94301b95e62cf2b20881a
Source noteuspto-grants-1979_07