HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74835Generated: October 30, 2026
Trichloroacetonitrile → HCID 86658274, compound
https://huagongshe.com/reaction/74835
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trichloroacetonitrile | HCID 11011 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | HCID 86658272 | HCID 86658272 | — |
| Catalyst | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86658274 | HCID 86658274 | 77% |
Reaction Steps
To a pre-cooled (0° C.) solution of 29 (609 mg, 0.569 mmol) in anhydrous DCM (2.8 mL, 0.2 M) was added trichloroacetonitrile (114 μL, 1.138 mmol, 2 eq). A solution of DBU (4.3 μL, 0.05 eq, 0.0285 mmol) in anhydrous DCM (0.3 mL) was added. The mixture was stirred at 0° C. for 4 h and TLC (hexane-EtOAc=65:35) indicated complete conversion. The crude mixture was evaporated onto silica gel and purified by silica column chromatography (2.5×14 cm, gradient elution with hexane-EtOAc-Et3N 210:20:0.5, 200:50:0.5, 180:60:0.5, 150:70:0.5). The product fractions were combined, evaporated and dried in a vacuum desiccator over P2O5 o/n to give the trichloroacetimidate 30 as white foam (530 mg, 77%), used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08828952B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-e985e81bec0c4735b7575a7351061dec |
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| Source note | uspto-grants-2014_09 |
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