HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 3-tert-butyl-4-((tert-butyldimethylsilyl)oxy)benzoate → 3-Tert-butyl-4-((tert-butyldimethylsilyl)oxy)benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 3-tert-butyl-4-((tert-butyldimethylsilyl)oxy)benzoate | HCID 18352492 | — |
| Reactant | Diisobutylaluminumhydride toluene | HCID 86583787 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Tert-butyl-4-((tert-butyldimethylsilyl)oxy)benzyl alcohol | HCID 53954164 | 90% |
Reaction Steps
According to example 184, 5.00 g of methyl 3-tert-butyl-4-((tert-butyldimethylsilyl)oxy)benzoate was reduced using 31.8 mL of 1M diisobutylaluminum hydride/toluene and 50 mL of anhydrous toluene. Analysis of the reaction mixture by tlc after 30 min indicated some remaining starting material. To ensure complete reduction, an additional 5 mL of 1M diisobutylaluminum hydride/toluene was added and the reaction was allowed to proceed for an additional 5 min. Work-up in the usual manner afforded 4.11 g (90%) of 3-tert-butyl-4-((tert-butyldimethylsilyl)oxy)benzyl alcohol as a cloudy oil. The product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06140100 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-c3b729b626ff4c30aff16de73400e83d |
| Source note | uspto-grants-2000_10 |