HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → Butyl 2-(tert-butyldimethylsilyloxy)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Butyl Glycolate | HCID 81882 | — |
| Solvent | Diethylether hexane | HCID 21584099 | — |
| Product | Butyl 2-(tert-butyldimethylsilyloxy)acetate | HCID 14079954 | — |
Reaction Steps
n-Butyl glycolate (231 g; 1.75 mol) and imidazole (345.1 g; 5.07 mol) are placed together at 0° C. The suspension obtained was treated portionwise with t-butyldimethylchlorosilane (303 g; 2.01 mol) during 1.5 hours. After 20 hours at room temperature the reaction mixture was diluted with ether/n-hexane 1:1 (1 l) and suction filtered. The crystals were rinsed thoroughly with ether/n-hexane 1:1 (200 ml). The filtrate was washed in succession with water (2×700 ml) and saturated aqueous sodium chloride solution (500 ml), dried over magnesium sulphate and concentrated. The oil obtained was distilled over a Vigreux column (7.5 cm). Yield: 405 g (94%) as a colourless oil (b.p. 78° C./0.98 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05464617 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-84479a15490745829d5c3b760057b4ea |
| Source note | uspto-grants-1995_11 |