HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromide ion → HCID 14974059, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | 3,3-Dimethyl-4-phenylbutan-2-one | HCID 83670 | — |
| Reactant | (3-Methoxy-2,2,3-trimethylbutyl)benzene | HCID 21218520 | — |
| Product | HCID 14974059 | HCID 14974059 | — |
Reaction Steps
Finally, 3-methoxy-2,2,3-trimethyl-1-phenylbutane (see line (3) of the scheme below) is prepared from 3,3-dimethyl-4-phenyl-2-butanone which is reacted with a methyl magnesium halide, e.g. the bromide or iodide, to obtain 2,3,3-trimethyl-4-phenyl-2-butanol. As in the synthesis described above for the other compounds of the invention, this alcohol is then etherified to obtain the desired product. ##STR1##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05939368 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-11996ac8bc644d599e751c6b10e1b443 |
| Source note | uspto-grants-1999_08 |