HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117367Generated: October 29, 2026
Trifluoroacetic acid → HCID 12069573, compound
https://huagongshe.com/reaction/2117367
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 12069571 | HCID 12069571 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | HCID 12069573 | HCID 12069573 | 87% |
Reaction Steps
2.32 ml of trifluoroacetic acid are added dropwise to a solution of 643 mg (1.51 mmol) of tert-butyl 3-(3-methoxy-4-nitrobenzoyl)-2-methylindolizin-1-ylcarbamate in 20 ml of dichloromethane, cooled to 0° C. Once the introduction is complete, the medium is allowed to return to room temperature and it is stirred for 4 hours. The reaction medium is poured over a saturated aqueous potassium carbonate solution and extracted with ethyl acetate. The organic phase is separated after settling out, washed with a saturated aqueous sodium chloride solution, dried over sodium sulphate and concentrated under reduced pressure. The crystals obtained are taken up in isopropyl ether, filtered off, washed with isopropyl ether and then dried. 425 mg of a brown solid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07442708B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-2700da04f660456cbc1545bb9fc4ee44 |
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| Source note | uspto-grants-2008_10 |
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