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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985897Generated: October 31, 2026

2,3-Difluorobenzaldehyde → HCID 66776591, compound

https://huagongshe.com/reaction/1985897

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DifluorobenzaldehydeHCID 137664—
Reactant1-(diethoxymethyl)-1H-imidazoleHCID 3849535—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66776591HCID 6677659164.6%

Reaction Steps

To a solution of 1-(diethoxymethyl)-1H-imidazole (1.65 ml, 10.1 mmol) in tetrahydrofuran (15 ml), at −60° C. and under nitrogen, was added n-butyllithium (2.5 M in hexanes, 4.03 ml, 10.1 mmol). The reaction mixture was stirred at −60° C. for 1 h, before addition of 2,3-difluorobenzaldehyde (1.00 ml, 9.2 mmol), and then allowed to warm to room temperature over 18 h. The mixture was concentrated in vacuo and to the residue was added ethyl acetate (50 ml) and hydrochloric acid (3M, 50 ml). The two layers were separated and the aqueous phase was basified with aqueous sodium hydroxide solution (20%) and extracted with ethyl acetate (3×100 ml). The combined organic phases were dried (MgSO4) and concentrated in vacuo and the residue was re-crystallised from 2-propanol to give the title compound (1.25 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547718B2
Source datasetuspto-grants-2009_06
ORD IDord-e8b7542c0c044d159a47da77f2b10905
Source noteuspto-grants-2009_06