HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 3,5-Bis(methoxymethoxy)benzyl tert-butyldimethylsilyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 3,5-Bis(methoxymethoxy)benzylalcohol | HCID 10443751 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,5-Bis(methoxymethoxy)benzyl tert-butyldimethylsilyl ether | HCID 9997516 | 97% |
Reaction Steps
To a solution of (3,5-bis-methoxymethoxy-phenyl)-methanol (220b) (290 g, 1.27 mol) and imidazole (129 g, 1.9 mol) in CH2Cl2 (1.5 L) was added TBSCl (286 g, 1.9 mol) at 5° C. in several portion was stirred at room temperature overnight. TLC (EtOAc/petroleum ether=1/2) showed that the reaction was complete. The mixture was filtered and the filtrate was washed with water, dried over Na2SO4 and concentrated under high vacuum to give the title compound (320 g, 97%) as a brown oil. 1H NMR (400 MHz, CDCl3): δ 6.68 (d, 2H), 6.57(t, 1H), 5.14 (s, 4H), 4.66 (s, 2H), 3.48 (s, 6H), 0.94 (s, 9H), 0.07 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119624B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-59ce6d2eb24144e89682b294515394be |
| Source note | uspto-grants-2012_02 |