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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470709Generated: October 29, 2026

Trichloroacetonitrile → HCID 86672614, compound

https://huagongshe.com/reaction/470709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetonitrileHCID 11011—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 70871896HCID 70871896—
SolventDichloromethaneHCID 6344—
ProductHCID 86672614HCID 8667261477%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629133B2
Source datasetuspto-grants-2014_01
ORD IDord-59b6e4bd919546cda8e1451d3ef7686d
Source noteuspto-grants-2014_01