HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246191Generated: October 31, 2026
Trichloroacetyl chloride → HCID 21914138, compound
https://huagongshe.com/reaction/1246191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trichloroacetyl chloride | HCID 6420 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 21914132 | HCID 21914132 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21914138 | HCID 21914138 | 83% |
Reaction Steps
Triethylamine (0.41291 mole) was added to intermediate (8) (0.08258 mole) suspended in dichloromethane (500 ml) at 0° C. Trichloroacetyl chloride (0.20645 mole) was added over 10 minutes. When the reaction appeared sluggish, an additional portion of triethylamine (20 ml) and then more trichloroacetyl chloride (7.6 ml) were added, and the mixture was stirred for 2 hours at low temperature. The ice bath was removed, and the mixture was allowed to sit for 2 hours. This resulted in a darker colored reaction, which was re-cooled to 0° C. Ice cold water (150 ml) was slowly added, and the mixture was stirred for 5 minutes. The layers were separated, and the organic phase was washed (ice cold 3N HCl, saturated NaHCO3), dried, filtered, and concentrated. The residue was triturated in ice cold diethylether (40 ml). Filtration, rinsing with ice cold diethylether (10 ml), yielding 15.13 g of 1-acetyl-5-chloro-2,3-dihydro-1H-indole-2-carbonitrile (intermediate 9, mp. 140–142° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07125891B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-cab645edf2be46a9ab006a72fd72dc6d |
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| Source note | uspto-grants-2006_10 |
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