HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-tert-Butyltoluene → 1-(Bromomethyl)-4-(1,1-dimethylethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-tert-Butyltoluene | HCID 7390 | — |
| Reactant | Bromine | HCID 24408 | — |
| Product | 1-(Bromomethyl)-4-(1,1-dimethylethyl)benzene | HCID 87836 | — |
Reaction Steps
In another known process in which a Cu salt is likewise used, i.e. Cu(NO3)2, p-tert.butyltoluene is the starting material, which is first reacted with an approximately equivalent amount of bromine to give p-tert.butylbenzyl bromide which is then boiled for a prolonged period of time in combination with a Cu(NO3)2 solution. p-tert.Butylbenzaldehyde is obtained in this manner in a yield of about 42% of the theory (cf. J. Chem. Soc., 1935, page 1848).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04277421 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-e3d033bc9a68418ea35c39a0f811cce2 |
| Source note | uspto-grants-1981_07 |