HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599376Generated: October 25, 2026
Trifluoroacetic acid → 2-(4-Nitrophenyl)ethyl pyrrolo[4,5-e]indoline-7-carboxylate
https://huagongshe.com/reaction/599376
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-(4-Nitrophenyl)ethyl3-[(tert-butyl)oxycarbonyl]pyrrolo[4,5-e]indoline-7-carboxylate | HCID 66717029 | — |
| Product | 2-(4-Nitrophenyl)ethyl pyrrolo[4,5-e]indoline-7-carboxylate | HCID 66717028 | — |
Reaction Steps
Two grams (4.43 mmol) of 14 are weighed into a round bottomed flask. Then, in a fume hood, 25 mL (325 mmol) of trifluroacetic acid is added, and the flask is capped and stirred. The solid dissolves in about a minute. The mixture is stirred for 1 hour, at which time deprotection will be done (HPLC can be used as a check). The acid is evaporated on a rotary evaporator (use a trap) and the product is dissolved in 100 mL of methylene chloride. This is extracted twice with 100 mL of half to ⅔ saturated sodium bicarbonate solution. The aqueous layers are back-extracted once with ˜50 mL of methylene chloride and this is combined with the rest. The organic layer is dried over sodium sulfate twice and evaporated to give a brown solid. If desired, this material can be recrystallized by diluting a very concentrated solution in methylene chloride with methanol and cooling.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897736B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-8b651f164a374d47a90f70e6a1bb924c |
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| Source note | uspto-grants-2011_03 |
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