HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2,4-Dibromo-beta-butylbenzeneethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 2,4-dibromo-alpha-butylbenzeneacetate | HCID 12343320 | — |
| Reactant | Lithium iodide (LiI), dihydrate | HCID 23688289 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2,4-Dibromo-beta-butylbenzeneethanol | HCID 12343364 | 100% |
Reaction Steps
A mixture of 16.5 parts of methyl 2,4-dibromo-α-butylbenzeneacetate, 11.5 parts of lithium iodide dihydrate and 180 parts of acetonitrile is stirred till all solid enters solution. Then there are added portionwise 3.6 parts of sodium borohydride. Upon completion, the whole is heated to reflux and stirring is continued overnight at reflux temperature. After cooling, the reaction mixture is acidified with a diluted hydrochloric acid solution and poured onto water. The product is extracted with 2,2'-oxybispropane. The extract is washed with water, dried, filtered and evaporated, yielding 15 parts (100%) of 2,4-dibromo-β-butylbenzeneethanol as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04598085 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-99f51b1d1de5474dab62edc6037e9488 |
| Source note | uspto-grants-1986_07 |