HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899016Generated: October 25, 2026
4-Hydroxybenzaldehyde → 4-Trimethylsilanylmethoxybenzaldehyde
https://huagongshe.com/reaction/899016
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Silane, (chloromethyl)trimethyl- | HCID 75361 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Trimethylsilanylmethoxybenzaldehyde | HCID 56528964 | 84% |
Reaction Steps
Chloromethyltrimethylsilane (110.5 g, 0.9 mol) is added dropwise over 30 minutes to a mixture of para-hydroxybenzaldehyde (110 g, 0.82 mol) and potassium carbonate (124.5 g, 0.9 mol) in 1 L of dry DMF maintained at 80° C., and while sparging with nitrogen. The mixture is left at 90° C. for 4 hours. The reaction mixture is filtered and the solvent is removed from the filtrate by distillation under vacuum. The final traces of DMF are removed via a stage at 60° C. under a vacuum of 2 mmHg. 142.4 g (yield: 84%) of 4-trimethylsilanylmethoxybenzaldehyde are obtained in the form of an orange-yellow oil, which is used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07354571B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-dfab117446f04b698ae0f92944dbd878 |
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| Source note | uspto-grants-2008_04 |
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