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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968796Generated: October 29, 2026

2,4,6-Trimethylbenzaldehyde → HCID 58625150, compound

https://huagongshe.com/reaction/1968796

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylbenzaldehydeHCID 10254—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 58625148HCID 58625148—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 58625150HCID 58625150—

Reaction Steps

Under N2, a mixture of [6-(3-aminomethyl-phenoxy)-3-propyl-3,4-dihydro-quinazolin-2-yl]-carbamic acid tert-butyl ester (0.0007 mol) and 2,4,6-trimethyl-benzaldehyde (0.0007 mol) in DCE (10 mL) was stirred at room temperature, then NaBH(OAc)3 (0.2 g) was added, and the reaction mixture was stirred overnight at room temperature. A saturated NaHCO3 solution was added, and the layers were separated. The organic layer was dried, filtered off and the solvent was evaporated. The residue was purified by Biotage column chromatography (gradient eluent: CH2Cl2:CH3OH). The purest product fractions were collected and the solvent was evaporated to yield the title compound as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426429B2
Source datasetuspto-grants-2013_04
ORD IDord-2e8d7a53c0f3462b93a30bab411101a2
Source noteuspto-grants-2013_04