HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910928Generated: November 3, 2026
Trichloroacetyl chloride → HCID 67367650, compound
https://huagongshe.com/reaction/1910928
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trichloroacetyl chloride | HCID 6420 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 67366177 | HCID 67366177 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67367650 | HCID 67367650 | 42.5% |
Reaction Steps
To a solution of ethyl 1-[2-(4-Chlorophenyl)-2-oxoethyl]-1H-pyrrole-2-carboxylate (150 mg, 0.54 mmol) in CH2Cl2 (10 ml) was added trichloroacetyl chloride (120 μL, 1.1 mmol) and aluminium chloride (290 mg, 2.2 mmol). After 16 h the reaction was quenched by the addition of a saturated aqueous solution of NaHCO3 (50 mL) and extracted with CH2Cl2 (3×50 mL). The organic extracts were combined, dried (MgSO4) and concentrated in vacuo to give a residue that was purified using flash chromatography (2× Biotage SP4, 12 g cartridge, 20-100% EtOAc gradient in n-hexanes) to give methyl 1-[2-(4-chlorophenyl)-2-oxoethyl]-4-(trichloroacetyl)-1H-pyrrole-2-carboxylate (97 mg, yield 42%) as a brown solid. 1H NMR (400 MHz, d6-acetone): δ 3.75 (s, 3H), 6.12 (s, 2H), 7.56 (d, 1H, J 2.0 Hz), 7.64-7.68 (m, 2H), 8.10-8.14 (m, 2H), 8.15 (d, 1H, J 2.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604034B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-4515d72340574940b2bc8551d29a5499 |
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| Source note | uspto-grants-2013_12 |
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