HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → Ethyl 2-[1-(t-butyldimethylsilyloxy)ethyl]acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Butanoic acid, 3-hydroxy-2-methylene-, ethyl ester | HCID 10855587 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 2-[1-(t-butyldimethylsilyloxy)ethyl]acrylate | HCID 14634473 | 95.5% |
Reaction Steps
To a suspension of ethyl 2-(1-hydroxyethyl)acrylate (40 g) and imidazole (28.3 g) in N,N-dimethylformamide (200 ml)was added portionwise t-butyldimethylsilyl chloride (46 g) at 0° C. After the mixture was stirred for 10 hours, the reaction mixture was poured into a mixture of water and ethyl acetate. The aqueous layer was separated and extracted twice with ethyl acetate. The combined organic layers were washed with water, 1N hydrochloric acid, saturated aqueous sodium hydrogencarbonate, water and an aqueous sodium chloride in turn, and then dried over magnesium sulfate. The evaporation of the solution gave ethyl 2-[1-(t-butyl-dimethylsilyloxy)ethyl]acrylate (68.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05241064 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-03f7eb77e5134ab59f6b5a9ed537e78c |
| Source note | uspto-grants-1993_08 |