HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389533Generated: October 31, 2026
2,4-Difluorobenzaldehyde → HCID 59400138, compound
https://huagongshe.com/reaction/2389533
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Difluorobenzaldehyde | HCID 73770 | — |
| Reactant | Boc-3-amino-1,2,3,4-tetrahydroquinoline | HCID 4460996 | — |
| Reactant | Tetramethylammonium Triacetoxyborohydride (>90%) | HCID 13696215 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 59400138 | HCID 59400138 | 97.5% |
Reaction Steps
To a solution of tert-butyl 1,2,3,4-tetrahydroquinolin-3-ylcarbamate (248 mg, 1.0 mmol) and 2,4-difluorobenzaldehyde (300 mg, 2.11 mmol) in 1,2-dichloroethane (10 mL) was added tetramethylammonium triacetoxyborohydride (0.6 g, 2.0 mmol). The mixture was stirred at 50° C. for 20 hours. The mixture was quenched by addition of saturated Rochelle's salt (10 mL) and extracted with dichloromethane (3×10 mL). The combined organic layers were washed with water (2×10 mL), dried over anhydrous sodium sulfate and evaporated to dryness. The residue was purified by chromatography on silica gel (5-40% EtOAc/Hexane) to give tert-butyl 1-(2,4-difluorobenzyl)-1,2,3,4-tetrahydroquinolin-3-ylcarbamate (365 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273754B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-c45f8df28ee245cfac8ffe1129365fe4 |
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| Source note | uspto-grants-2012_09 |
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