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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990383Generated: November 1, 2026

4-tert-Butylbenzaldehyde → HCID 59913957, compound

https://huagongshe.com/reaction/990383

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylbenzaldehydeHCID 70324—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 12017817HCID 12017817—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 59913957HCID 5991395773%

Reaction Steps

(S)-2-Amino-1-{4-[bis-(4-fluoro-phenyl)-methyl]-piperazin-1-yl}-4-methyl-pentan-1-one (0.500 g, 1.25 mmol, Example 53) and 4-(tert-butyl)benzaldehyde (0.208 mL, 1.25 mmol, Aldrich, Milwaukee, Wis.) were mixed in CH2Cl2 (6 mL). After stirring at ambient temperature under nitrogen atmosphere for 30 minutes, the solution was cooled to 0° C. in an ice-water bath. To this solution was added sodium triacetoxyborohydride (0.396 g, 1.87 mmol). The resulting reaction mixture was stirred for, in succession, 30 minutes at 0° C. and 12 hours at ambient temperature. Twenty milliliters of saturated aqueous NaHCO3 solution was added to the reaction mixture and the resulting mixture was stirred for 15 minutes. The two layers were separated and the aqueous layer was extracted with CH2Cl2 (2×20 mL). The combined organic solution was dried over Na2SO4. TLC (50% EtOAc in Hexanes as the eluant) showed two spots with Rf values 0.93 and 0.63. The solution was concentrated in vacuo affording a viscous oil. The lower spot on TLC (Rf=0.63) was isolated by flash chromatography (30% EtOAc in hexanes). 0.496 g (73%) of the pure titled compound was obtained as a white foam: mp 57-62° C. APCI-MS m/z 548.5 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458781B1
Source datasetuspto-grants-2002_10
ORD IDord-6e0cfbf9580643e09cff3ceb37db80c6
Source noteuspto-grants-2002_10