HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853049Generated: October 28, 2026
Trifluoroacetic acid → HCID 11816794, compound
https://huagongshe.com/reaction/853049
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 11392958 | HCID 11392958 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11816794 | HCID 11816794 | 76.6% |
Reaction Steps
7-Ethyl-indole-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester (76.6 g, 0.24 mol was dissolved in 450 mL dichloromethane and cooled to 0° C. Trifluoroacetic acid (150.0 mL, 1.96 mol) was added within 30 min. and after an additional 45 min. the reaction mixture was concentrated at a rotary evaporator. The residue was dissolved in 300 mL dichloromethane and poured cautiously onto 500 mL saturated aq. sodium bicarbonate solution. The phases were separated and the aqueous phase was extracted twice with dichloromethane. The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated on a rotary evaporator. The residue was suspended in 400 mL n-hexane and put in an ultrasonic bath for 15 min. The suspension was filtered and the filter cake was washed with 100 mL n-hexane. This procedure was repeated to give the desired product as a light brown solid (40.2 g, 76.6%). EI-MS: m/e=217.1 ([M])
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253281B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-2bbfe52d7e374a1196114958408c5a4b |
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| Source note | uspto-grants-2007_08 |
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