HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → Ethyl 3-((tert-butyldimethylsilyl)oxy)hexanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Ethyl 3-hydroxyhexanoate | HCID 61293 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 3-((tert-butyldimethylsilyl)oxy)hexanoate | HCID 14264095 | 82% |
Reaction Steps
A solution of ethyl 3-hydroxyhexanoate 1 (2.0 g, 12.5 mmol), imidazole (1.09 g, 18.7 mmol), and tert-butyldimethylsilyl chloride (2.26 g, 15.0 mmol) in DMF (25 mL) was stirred at 23° C. After 16 h the reaction was diluted with Et2O and then washed with 1N HCl, saturated aqueous NaHCO3 and brine. The organic portion was dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by flash column chromatography (silica gel, 100% hex followed by 19:1 hex/EtOAc) afforded 2.8 g (82%) of silyl ether 2 (see Scheme 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09315486B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-7f65529dc22c4fb1bd9fece3faf73783 |
| Source note | uspto-grants-2016_04 |