Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301665Generated: October 31, 2026

Trifluoroacetic acid → HCID 18373253, compound

https://huagongshe.com/reaction/2301665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 11580537HCID 11580537—
ReactantHCID 18373335HCID 18373335—
SolventDichloromethaneHCID 6344—
ProductHCID 18373253HCID 1837325389%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 1-benzhydryl-6-chloro-1H-indole (1.0 eq) and methyl 2-(4-formyl-2,6-dimethylphenoxy)acetate (0.6 eq) in CH2Cl2 (0.1M) at 0° C. was added neat triethysilane (3 eq) followed by triflouroacetic acid (3 eq). After 10 minutes at 0° C. the reaction was warmed to room temperature and stirred until the initially formed spot by TLC yields a new spot. The reaction was then quenched by the addition of saturated sodium bicarbonate, diluted with CH2Cl2 and washed with saturated sodium bicarbonate, water and brine, dried over magnesium sulfate and purified by column chromatography to yield 89% of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500853B1
Source datasetuspto-grants-2002_12
ORD IDord-c6d28c2096ae4d89a8683f7288004d1a
Source noteuspto-grants-2002_12