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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551908Generated: October 28, 2026

4-tert-Butylbenzaldehyde → HCID 11585104, compound

https://huagongshe.com/reaction/551908

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylbenzaldehydeHCID 70324—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant6-({4-[(4-butylphenyl)ethynyl]benzyl}amino)-2,2-dimethyl-4H-1,3-benzodioxin-4-oneHCID 11476168—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 11585104HCID 1158510435.6%

Reaction Steps

To a solution of 6-({4-[(4-butylphenyl)ethynyl]benzyl}amino)-2,2-dimethyl-4H-1,3-benzodioxin-4-one (150 mg, 0.34 mmol) in anhydrous DCE (3 mL) were added 4-tert-butylbenzaldehyde (Aldrich, 85 μL, 0.51 mmol) and sodium triacetoxyborohydride (110 mg, 0.51 mmol). The reaction mixture was stirred at rt for 72 hrs. The solvent was removed under reduced pressure. The residue was taken up with an aqueous solution of NaOH (2 mL, 1N) and extracted with Et2O (6 ml). The organic layer was dried over Na2SO4 and the solvent was removed under reduced pressure. Purification by flash chromatography on silicagel (pentane/DCM (2/3)) gave 71 mg (31%) of the title compound as a yellow oil. HPLC, Rt: 6.4 min (purity: 86.3%). 1H NMR (CDCl3) δ: 7.85-6.90 (m, 15H), 4.62 (brs, 4H), 2.62 (t, J=7.6 Hz, 2H), 1.70 (s, 6H), 1.61 (m, 2H), 1.33 (m, 2H), 1.30 (s, 9H), 0.93 (t, J=7.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947851B2
Source datasetuspto-grants-2011_05
ORD IDord-b073b74e4e774ea4aaa107e36d17009d
Source noteuspto-grants-2011_05