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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064979Generated: October 30, 2026

Nitrogen → Benzaldehyde, 3-(2-methyl-1,3-dioxolan-2-yl)-

https://huagongshe.com/reaction/2064979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(3-Bromophenyl)-2-methyl-1,3-dioxolaneHCID 10999218—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductBenzaldehyde, 3-(2-methyl-1,3-dioxolan-2-yl)-HCID 10607757—

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), to a solution of 2-(3-bromo-phenyl)-2-methyl-[1,3]dioxolane (944 mg, 3.88 mmol) in THF (20.0 mL) at −78° C. was added dropwise n-BuLi (1.60 mL of a 2.5M solution in hexane, 4.00 mmol). The reaction mixture was then stirred at −78° C. for 30 min before DMF (0.40 mL, 5.17 mmol) was added dropwise. The reaction mixture was allowed to warm to rt over 1 h. Sat. aq. NH4Cl was added and the mixture was extracted three times with Et2O. The combined org. extracts were dried over Na2SO4, filtered, and the solvent was removed under reduced pressure to give the crude title compound as a pale yellow oil. LC-MS-conditions 02: tR=0.87 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288419B2
Source datasetuspto-grants-2012_10
ORD IDord-2f7f25f648ab4c1f971909437d1cc268
Source noteuspto-grants-2012_10