HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → Rac-[(1r,4r)-4-{[(tert-butyldimethylsilyl)oxy]methyl}cyclohexyl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | 1,4-Cyclohexanedimethanol | HCID 7735 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Rac-[(1r,4r)-4-{[(tert-butyldimethylsilyl)oxy]methyl}cyclohexyl]methanol | HCID 10753723 | 57% |
Reaction Steps
To a solution of cyclohexane-1,4-dimethanol (10.0 g) in N,N-dimethylformamide (100 mL) were added successively tert-butyldimethylchlorosilane (8.9 g) and imidazole (9.5 g), followed by stirring the reaction mixture at room temperature for 16 hours. To the reaction mixture were added ice and saturated aqueous lithium bromide solution, followed by extraction with diethyl ether. The organic layer was washed with saturated aqueous lithium bromide solution and saturated brine, dried and concentrated. The residue was purified by column chromatography on silica gel (ethyl acetate:hexane (volume ratio)=1:9 to 2:3) to give [4-(tert-butyldimethylsilanyloxymethyl)-cyclohexyl]-methano 1 (8.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08299296B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-72f6a98c68994e669277ac8ac7d92b24 |
| Source note | uspto-grants-2012_10 |