Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556142Generated: October 29, 2026

Potassium tert-butoxide → HCID 131729272, compound

https://huagongshe.com/reaction/556142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 131729267HCID 131729267—
SolventTolueneHCID 1140—
ProductHCID 131729272HCID 13172927266.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

Firstly, PPh3MeI (317 mg, 0.78 mmol: Me=methyl) was added with dist. toluene (4 mL). The resultant mixture was then added with KOt-Bu (88 mg, 0.78 mmol) at 0° C., and then was stirred under a nitrogen atmosphere at 0° C. for 30 minutes to obtain a mixture. Subsequently, the obtained mixture was added dropwise with a mixed solution (2 mL) of 4-(diallylethoxysilyl)benzaldehyde (204.2 mg, 0.78 mmol) obtained in Example 12 and dist. toluene under a nitrogen atmosphere at 0° C. The resultant mixture was stirred under a nitrogen atmosphere at 0° C. for 1.5 hours, and then was stirred at room temperature for 17 hours to obtain a reaction mixture. After that, a salt contained in the reaction mixture was removed through a celite filtration process. The organic layer thus obtained was then concentrated under reduced pressure to obtain a crude product. The obtained crude product was separated and purified by silica gel column chromatography (hexane/EtOAc=20/1) to obtain 4-(diallylethoxysilyl)styrene (134.3 mg, 66% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053588B2
Source datasetuspto-grants-2011_11
ORD IDord-c4b46053c88b459ea9346a072295234c
Source noteuspto-grants-2011_11