HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → (1S,3S)-3-({[tert-butyl(dimethyl)silyl]oxy}methyl)cyclopentanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 3-(Hydroxymethyl)cyclopentanol | HCID 58651115 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (1S,3S)-3-({[tert-butyl(dimethyl)silyl]oxy}methyl)cyclopentanol | HCID 66797963 | 31% |
Reaction Steps
To a solution of (1S,3S)-3-(hydroxymethyl)cyclopentanol (453.0 mg, 0.003276 mol) and 1H-imidazole (669 mg, 0.00983 mol) in DMF (35.8 mL) under an atmosphere of nitrogen was added tert-butyldimethylsilyl chloride (494 mg, 0.00328 mol). The mixture was stirred for 1.25 hours, then tert-butyldimethylsilyl chloride (49 mg, 0.00033 mol) was added. After an additional hour of stirring, the reaction was quenched with water, extracted with ethyl acetate (3×), dried with anhydrous Na2SO4, filtered, and concentrated. The residue was filtered through a plug of silica with 30% EtOAc/hexanes to obtain 234.1 mg (31%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08008307B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-ce3c0f8818d44e0c92ed64ebf8c21344 |
| Source note | uspto-grants-2011_08 |