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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74835Generated: October 30, 2026

Trichloroacetonitrile → HCID 86658274, compound

https://huagongshe.com/reaction/74835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetonitrileHCID 11011—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 86658272HCID 86658272—
Catalyst1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventDichloromethaneHCID 6344—
ProductHCID 86658274HCID 8665827477%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828952B2
Source datasetuspto-grants-2014_09
ORD IDord-e985e81bec0c4735b7575a7351061dec
Source noteuspto-grants-2014_09