HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470709Generated: October 29, 2026
Trichloroacetonitrile → HCID 86672614, compound
https://huagongshe.com/reaction/470709
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trichloroacetonitrile | HCID 11011 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 70871896 | HCID 70871896 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86672614 | HCID 86672614 | 77% |
Reaction Steps
1,8-Diazabicyclo[5.4.0]undec-7-ene (1.00 ml, 6.83 mmol) was added to a dichloromethane (22 ml) solution of the compound (6.83 mmol) obtained in Step 2 above combined with trichloroacetonitrile (0.82 ml, 8.20 mmol) under ice cooling and the resulting mixture was stirred at room temperature for 1 hour. The solvent in the reaction mixture was evaporated under reduced pressure and the residue was dissolved in chloroform and added dropwise into n-hexane:ethyl acetate [4:1 (v/v)] mixed solvent. The resulting insoluble matter was removed by filtration through celite and the solvent in the filtrate was evaporated under reduced pressure. The residue obtained was purified by silica gel column chromatography [n-hexane:ethyl acetate=99:1→10:1 (v/v)] to give 2.1 g (77%) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629133B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-59b6e4bd919546cda8e1451d3ef7686d |
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| Source note | uspto-grants-2014_01 |
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