HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735172Generated: October 31, 2026
Carbon Dioxide → 3-(Trimethylsilyl)butanoic acid
https://huagongshe.com/reaction/1735172
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 3-Bromopropyltrimethylsilane | HCID 12845800 | — |
| Product | 3-(Trimethylsilyl)butanoic acid | HCID 19437022 | — |
Reaction Steps
A solution containing 3 g (15.4 mmol) of (3-bromopropyl)trimethylsilane in 3 ml of dry ether was added to 0.375 g (15.4 mmol) of magnesium turnings in ether (40 ml final volume of solution). After 1 hour of reflux gazeous carbondioxide was bubbled through the reaction mixture (3 g, 77 mmol of dry ice). After 2 hours of stirring at room temperature the reaction mixture was partitioned between aqueous ammonium chloride and ether. The organic phase was separated, the aqueous phase was further acidified with hydrochloric acid 1N and extracted with ether. Ethereal phases were pooled and the solvent was removed under reduced pressure. Separation of the expected 4-trimethylsilyl-butanoic acid from dimer of starting (3-bromopropyl)trimethylsilane was finally performed by acid base extraction. 0.62 g of 3-(trimethylsilyl)-butanoic acid was isolated as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05536732 |
|---|
| Source dataset | uspto-grants-1996_07 |
|---|
| ORD ID | ord-93d3d9900d134dd1922301639c5f8877 |
|---|
| Source note | uspto-grants-1996_07 |
|---|