Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862070Generated: October 25, 2026

Dimethylformamide → 5-(2-Trimethylsilylethynyl)-2-methoxymethoxybenzaldehyde

https://huagongshe.com/reaction/862070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthyl AcetateHCID 8857—
Reactant(4-Methoxymethoxy-phenylethynyl)-trimethylsilaneHCID 10657368—
ReactantHCID 178446069HCID 178446069—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product5-(2-Trimethylsilylethynyl)-2-methoxymethoxybenzaldehydeHCID 19701592—

Reaction Steps

A solution of 4-(2-trimethylsilylethynyl)phenol methoxymethyl ether (6.08 g) in diethyl ether (450 ml) was cooled to -78° C., to which was added dropwise, under argon atmosphere, a 1.7M t-butyl lithium pentane solution (18 ml), and the mixture was stirred for one hour at the same temperature. To the reaction mixture was then added dropwise DMF(5 ml), followed by warming up to room temperature and stirring overnight. To the reaction mixture were added ethyl acetate and water, which was subjected to extraction. The organic layer was washed (a saturated aqueous saline solution) and dried (anhydrous magnesium sulfate), followed by distilling off the solvent under reduced pressure. The residue was purified by means of a silica gel column chromatography (eluted with ethyl acetate/hexane) to give 5-(2-trimethylsilylethynyl)-2-methoxymethoxybenzaldehyde (5.29 g) (Compound B-27). The physical properties are shown in Table 8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05716971
Source datasetuspto-grants-1998_02
ORD IDord-01eb2cf2a43c4d479d27f41b864bad98
Source noteuspto-grants-1998_02