HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 2,3-Dimethyl-2-butene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | InChI=1/C6H15B/c1-5(2)6(3,4)7/h5H,7H2,1-4H | HCID 5326179 | — |
| Product | 2,3-Dimethyl-2-butene | HCID 11250 | — |
| Product | Borane;tetrahydrofuran | HCID 2723981 | — |
Reaction Steps
A 10 mL round-bottomed flask was charged with 5-carbon linked dimer alcohol (57 mg, 0.0885 mmol) in 1 mL of THF. To the reaction mixture was added thexylborane (0.8 mL, 3 eq.) 0.33M in THF solution obtained from BH3THF (1 eq) and 2,3-dimethyl-2-butene (2 eq) at 0° C. for 1 hr. The reaction mixture was stirred for 2 hr and then added 3 N NaOH (0.15 mL, 5 eq) and 30% H2O2 (0.15 mL, 5 eq). The reaction mixture was warmed to room temperature and then stirred for 12 hr. The reaction mixture was quenched with H2O, extracted with EtOAc, dried over MgSO4 and concentrated. The crude product was purified by column chromatography (EtOAc/Hexane=3/1) to give 39.2 mg in 65% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08884032B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-bb61b7929eb245cab96fc434a5f22a00 |
| Source note | uspto-grants-2014_11 |