HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301665Generated: October 31, 2026
Trifluoroacetic acid → HCID 18373253, compound
https://huagongshe.com/reaction/2301665
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | HCID 11580537 | HCID 11580537 | — |
| Reactant | HCID 18373335 | HCID 18373335 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18373253 | HCID 18373253 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06500853B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-c6d28c2096ae4d89a8683f7288004d1a |
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| Source note | uspto-grants-2002_12 |
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