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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dichlorobenzoyl chloride | HCID 17944 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 7-Bromo-2-methylindole | HCID 4413081 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69527429 | HCID 69527429 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06995184B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-5ce1e6b06a7f4830b3fa846e36948413 |
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| Source note | uspto-grants-2006_02 |
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