HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556129Generated: October 29, 2026
Hydrochloric Acid → HCID 131729267, compound
https://huagongshe.com/reaction/556129
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 131727682 | HCID 131727682 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Reactant | HCID 178443870 | HCID 178443870 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131729267 | HCID 131729267 | 85% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08053588B2 |
|---|
| Source dataset | uspto-grants-2011_11 |
|---|
| ORD ID | ord-8dde3e98a72c4a8e9546c577bfc3f724 |
|---|
| Source note | uspto-grants-2011_11 |
|---|