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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556129Generated: October 29, 2026

Hydrochloric Acid → HCID 131729267, compound

https://huagongshe.com/reaction/556129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantHCID 131727682HCID 131727682—
ReactantHCID 178418918HCID 178418918—
ReactantHCID 178443870HCID 178443870—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131729267HCID 13172926785%

Reaction Steps

Firstly, i-PrMgCl (0.71 mL, 2 M in THF, 1.42 mmol) was added dropwise to a THF solution (2 mL) of 4-(diallylethoxysilyl)iodobenzene (255 mg, 0.71 mmol) obtained in Synthesis example 7 at −30° C. The resultant mixture was stirred under a nitrogen atmosphere at −30° C. for 1.5 hours to obtain a solution containing 4-(diallylethoxysilyl)phenylmagnesium chloride (Grignard solution). Then, DMF (110 μL, 1.42 mmol) was added dropwise to the obtained solution at −30° C., and the resultant mixture was stirred under a nitrogen atmosphere at room temperature for 13 hours to obtain a reaction mixture. Subsequently, an aqueous solution of HCl of 10% by mass was added to the reaction mixture to cease the reaction. After that, an organic layer was separated from the reaction mixture, and an aqueous layer was extracted with ether. The organic layer thus collected was washed with sat. NaHCO3 and sat. NaCl, and dried with MgSO4. The dried organic layer was filtered and concentrated to obtain a crude product. The crude product was separated and purified by silica gel column chromatography (hexane/EtOAc=20/1) to obtain 4-(diallylethoxysilyl)benzaldehyde (158 mg, 85% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053588B2
Source datasetuspto-grants-2011_11
ORD IDord-8dde3e98a72c4a8e9546c577bfc3f724
Source noteuspto-grants-2011_11