HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzaldehyde → 4-((2-Methyl-2-propyl)diphenylsilyloxy)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-((2-Methyl-2-propyl)diphenylsilyloxy)benzaldehyde | HCID 11428383 | — |
Reaction Steps
At 0° C., tert-butyldiphenylchlorosilane (50 g) was added slowly to a solution of p-hydroxybenzaldehyde (22 g) and Et3N (42 mL) in 1,2-dichloroethane (400 mL) and the mixture was stirred at room temperature a few hours. After the usual work up, the product was purified by flash chromatography on silica using EtOAc:hexane 1:10 and was used as such for Step 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05232916 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-3fadddfa39964ab886d131b58d7a7e72 |
| Source note | uspto-grants-1993_08 |