HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-3-methylbutane → 15-Methylhexadecyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-3-methylbutane | HCID 7891 | — |
| Reactant | 1,12-Dibromododecane | HCID 18766 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Catalyst | Copper;dilithium;tetrachloride | HCID 193501 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 15-Methylhexadecyl bromide | HCID 20437385 | — |
| Product | HCID 178418529 | HCID 178418529 | — |
Reaction Steps
A solution of 3-methylbutylmagnesium bromide is prepared by treating 15 g. (0.1 mole) 3-methylbutyl bromide with 2.7 g. (1.1 eq) magnesium turnings in 50 ml. dry tetrahydrofuran. The resultant Grignard reagent is dropwise added to a cold (-10° C.) solution of 36.1 g. (1.1 eq) 1,12-dibromododecane and 0.2 g. (1 m mole) dilithiumtetrachloro cuprate in 75 ml. dry tetrahydrofuran. The solution is stirred for one hour, evaporated, and fractionally distilled in vacuo to yield 15-methylhexadecylbromide as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04254138 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-4b450992ea5c48be9f42825b1c6d7949 |
| Source note | uspto-grants-1981_03 |