HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisobutylaluminumhydride → HCID 23442890, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 23442893 | HCID 23442893 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 23442890 | HCID 23442890 | 84.5% |
Reaction Steps
Under a nitrogen stream, 0.15 g of 6-t-butyl-2-methy-5-trimethylacetoxy-2,3-dihydrobenzofuran was dissolved in 3 ml of n-hexane at room temperature, 1.55 ml of diisobutylaluminium hydride (1M in n-hexane) was added dropwise, and the mixture was stirred overnight. After the reaction was quenched with 5% hydrochloric acid, the mixture was extracted with water and ethyl acetate. The organic layers were washed with saturated brine, dried over anhydrous magnesium sulfate and then concentrated. The concentrate was purified on a short column of silica gel (in n-hexane containing 5% ethyl acetate) to give 0.09 g of 6-t-butyl-5-hydroxy-2-methyl-2,3-dihydrobenzofuran as a white solid (yield 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06686389B2 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-872efd7dfb2e4a409a08bf9ab945803d |
| Source note | uspto-grants-2004_02 |