HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429666Generated: November 1, 2026
4-Fluorobenzaldehyde → HCID 16660608, compound
https://huagongshe.com/reaction/1429666
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Triacetoxyborohydride | HCID 2724942 | — |
| Reactant | HCID 59805851 | HCID 59805851 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 16660608 | HCID 16660608 | 42% |
Reaction Steps
A suspension of D2 (1.7 g, 5.32 mmol), 4-fluorobenzaldehyde (0.66 g, 5.32 mmol), di-isopropylethylamine (1.37 g, 10.6 mmol) and triacetoxyborohydride on resin (Argonaut Technologies; 2.2 mmol/g; 3 eq.) in dichloroethane (10 ml) was stirred at room temperature for 18 h. After this period, the reaction mixture was filtered and the solvents evaporated in vacuo. The crude product was purified by chromatography (silica; 2%-6% ammonia in methanol (7 M)/dichloromethane) to give E2 (0.79 g, 42%). C17H18F4N4 requires 354; Found 355 (MH+); mp: 163.3-165.3° C. 1H NMR (DMSO-D6) δ 1.48 (q, J=10.8 Hz, 2H), 1.95 (br.d, J=12.5 Hz, 2H), 2.09 (t, J=11.1 Hz, 2H), 2.78 (br.d, J=11.3 Hz, 2H), 3.47 (s, 2H), 3.89 (br.s, 1H), 6.94 (d, J=9.4 Hz, 1H), 7.15 (t, J=8.8 Hz, 2H), 7.34 (dd, J=8.3, 5.7 Hz, 2H), 7.53 (br.d, J=7.3 Hz, 1H), 7.63 (d, J=9.4 Hz, 1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940743B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-d8838f7cea1346118231ca412267fbd6 |
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| Source note | uspto-grants-2015_01 |
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