HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-tert-Butyl-4-hydroxyanisole → 2-tert-Butyl-4-hydroxyanisole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-tert-Butyl-4-hydroxyanisole | HCID 6932 | — |
| Reactant | Tert-Butylhydroquinone | HCID 16043 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-tert-Butyl-4-hydroxyanisole | HCID 6932 | — |
| Product | Butylated Hydroxyanisole | HCID 8456 | — |
Reaction Steps
5.0 g of tert-butyl-hydroquinone, 40 cm3 of methanol and 1.0 g of cupric chloride are fed into the autoclave. The autoclave is purged with nitrogen and kept at 105° C. for 2.5 hours. On termination of the reaction, mixture analysis indicates the formation of 4.4 g of tert-butyl-hydroquinone monomethyl ether (BHA) (conversion 100%, selectivity 82%). The two BHA isomers (3-tert-butyl-4-hydroxyanisole and 2-tert-butyl-4-hydroxyanisole) are formed in a weight ratio of 99:1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04469897 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-0a1acd4bef8c441bb685e10cda75f930 |
| Source note | uspto-grants-1984_09 |