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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429666Generated: November 1, 2026

4-Fluorobenzaldehyde → HCID 16660608, compound

https://huagongshe.com/reaction/1429666

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantDiisopropylethylamineHCID 81531—
ReactantTriacetoxyborohydrideHCID 2724942—
ReactantHCID 59805851HCID 59805851—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 16660608HCID 1666060842%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940743B2
Source datasetuspto-grants-2015_01
ORD IDord-d8838f7cea1346118231ca412267fbd6
Source noteuspto-grants-2015_01