HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 4-tert-Butyldimethylsilyloxybenzeneacetic Acid Methyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Benzeneacetic acid, 4-hydroxy-, methyl ester | HCID 518900 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-tert-Butyldimethylsilyloxybenzeneacetic Acid Methyl Ester | HCID 13753416 | — |
Reaction Steps
A solution of 4-hydroxyphenylacetic acid methyl ester (2000 mg, 12036 μmol), 1H-imidazole (2048 μl, 18053 μmol), and chloro-tert-butyldimethylsilane (1814 mg, 12036 μmol) in DMF (10 mL) was stirred at 23° C. for 18 h. The mixture was partitioned between EtOAc (50 mL) and 5% NaHCO3 (25 mL). The organic layer was dried over MgSO4 and concentrated to a colorless oil from toluene under reduced pressure. MS (ESI pos. ion) m/z (MH+): 281. Calc'd exact mass for C15H24O3Si: 280.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08314087B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-c7c454d95dec460d8e7017c8c08b3aa6 |
| Source note | uspto-grants-2012_11 |