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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890242Generated: November 1, 2026

2,3-Dichlorobenzoyl chloride → HCID 69527429, compound

https://huagongshe.com/reaction/890242

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichlorobenzoyl chlorideHCID 17944—
ReactantAmmonium ChlorideHCID 25517—
Reactant7-Bromo-2-methylindoleHCID 4413081—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69527429HCID 69527429—

Reaction Conditions

Temperature-10 °C

Reaction Steps

10.7 g of 7-bromo-2-methyl-1H-indole are placed in 100 ml of THF and the mixture is cooled to −10° C. 22 ml of 3M methylmagnesium bromide in ether are added at this temperature. The mixture is allowed to return to AT and is then cooled to −5° C. and 13.5 g of 2,3-dichlorobenzoyl chloride, dissolved in 80 ml of THF, are added dropwise. The medium is allowed to return to AT and is then poured onto a saturated NH4Cl solution. Extraction is carried out with ether and then the organic phase is washed with a 10% NaOH solution, water and a saturated NaCl solution. It is dried and evaporated and the residue is chromatographed on silica while eluting with an AcOEt/cyclohexane (10/90, v/v) mixture. The product obtained crystallizes from ether and 5 g of the expected compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995184B2
Source datasetuspto-grants-2006_02
ORD IDord-5ce1e6b06a7f4830b3fa846e36948413
Source noteuspto-grants-2006_02