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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357267Generated: November 2, 2026

Oxalyl chloride → HCID 18505311, compound

https://huagongshe.com/reaction/1357267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 18505279HCID 18505279—
SolventDichloromethaneHCID 6344—
ProductHCID 18505311HCID 18505311—

Reaction Steps

Oxalyl chloride (5.89 mL, 66.1 mmol) was added under nitrogen to a solution of 2-butyl-1-methyl-1H-indole-3-carboxylic acid (3.06 g, 13.2 mmol), prepared in the previous step, in 100 mL of methylene chloride at room temperature. There was an immediate evolution of gas. After the addition the reaction was stirred at room temperature for 2 h. The solvent was removed under reduced pressure. To remove excess oxalyl chloride the residue was dissolved in benzene and the solvent removed under reduced pressure to give 2-butyl-1-methyl-1H-indole-3-carbonyl chloride as a brown oil. The material was immediately used without additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06589970B2
Source datasetuspto-grants-2003_07
ORD IDord-31d5ba508d964e8a85336d9badc4db67
Source noteuspto-grants-2003_07