HuagongsheHuagongshe Chemistry Print Report · For research reference only
t-Butyl bromide → 2,2,4,4-Tetramethylpentan-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | t-Butyl bromide | HCID 10485 | — |
| Reactant | Pivalaldehyde | HCID 12417 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,2,4,4-Tetramethylpentan-3-ol | HCID 139790 | — |
Reaction Steps
A solution of t-butyl bromide in ether is added slowly to magnesium stirrings until the Grignard reagent begins to form. The remainder of the alkyl bromide is then added and the mixture is stirred until all the magnesium dissolves. At 0° C., a solution of 2,2-dimethylpropionaldehyde is added and the resulting product is quenched with 1M HCl and extracted with ether and the solvent is evaporated to afford di-t-butylmethyl alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04652457 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-7023021dbc684064a563dcb6abddc484 |
| Source note | uspto-grants-1987_03 |