HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667274Generated: October 31, 2026
3-Fluoro-4-(trifluoromethyl)benzaldehyde → HCID 45274410, compound
https://huagongshe.com/reaction/1667274
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Fluoro-4-(trifluoromethyl)benzaldehyde | HCID 2737537 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 53391428 | HCID 53391428 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 45274410 | HCID 45274410 | — |
Reaction Steps
To a solution of N-azetidin-3-yl-2-[3,3-bis(4-fluorophenyl)-2-oxopyrrolidin-1-yl]acetamide (0.083 g, 0.215 mmol; Example 239A) in dichloromethane (5 mL) was added 3-fluoro-4-(trifluoromethyl)benzaldehyde (0.062 g, 0.323 mmol), sodium triacetoxyborohydride (0.088 g, 0.323 mmol) and a few drops of acetic acid. The reaction mixture was stirred at ambient temperature for 16 hours. The mixture was then diluted with dichloromethane and washed with saturated aqueous NaHCO3 solution. The separated organic layer was dried over MgSO4, concentrated, and purified by silica gel flash chromatography eluting with 5-10% methanol/dichloromethane. 1H NMR (300 MHz, CDCl3) δ ppm 7.54 (t, J=7.6 Hz, 1H), 7.28-7.33 (m, 4H), 7.12-7.16 (m, 2H), 6.98-7.05 (m, 4H), 6.30-6.37 (m, 1H), 4.40-4.59 (m, 1H), 3.99 (s, 2H), 3.54-3.66 (m, 4H), 3.50 (t, J=6.5 Hz, 2H), 2.77 (t, J=6.4 Hz, 4H); MS (ESI+) m/z 562 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044069B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-5ce951c2ffa24cbba71eea8d0b157808 |
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| Source note | uspto-grants-2011_10 |
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