HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178259Generated: October 29, 2026
Trifluoroacetic acid → HCID 59418746, compound
https://huagongshe.com/reaction/2178259
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 59418739 | HCID 59418739 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59418746 | HCID 59418746 | — |
Reaction Steps
Trifluoroacetic acid (18 mL) was added to tert-butyl 7-(6-(methoxycarbonyl)-5-(trifluoromethylsulfonyloxy)pyridin-2-yl)-3,4-dihydroquinoline-1(2H)-carboxylate (29E) (2.00 g, 3.9 mmol) in anhydrous DCM (25 mL). The reaction mixture was stirred at rt for 1.5 hours, concentrated under reduced pressure, diluted with DCM, and washed with saturated NaHCO3. The aqueous phase was extracted with DCM. The combined organic phases were dried over MgSO4, filtered, and concentrated under reduced pressure to provide the desired product methyl 6-(1,2,3,4-tetrahydroquinolin-7-yl)-3-(trifluoromethylsulfonyloxy)picolinate (29F) in sufficient purity for subsequent use. 1H NMR (300 MHz, CDCl3) δ 7.88 (1H d), 7.66 (1H, d), 7.39 (1H, d) 7.29 (1H, dd), 7.08 (1H, d), 4.03 (3H, s), 3.39 (2H, m), 2.83 (2H, t), 2.02 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067928B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-875814a86c0745e28ceb24714c23457c |
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| Source note | uspto-grants-2015_06 |
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