HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-tert-Butylphenol → 2-(4-Chloro-alpha-cumyl)-4-tert-butylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-tert-Butylphenol | HCID 7393 | — |
| Reactant | 4-Chloro-alpha-methylstyrene | HCID 74381 | — |
| Product | 2-(4-Chloro-alpha-cumyl)-4-tert-butylphenol | HCID 22664358 | — |
Reaction Steps
4-Chloro-α-methylstyrene (50 g) and 45 g of 4-tert-butylphenol are reacted according to the procedure of Example 3 to afford the title compound in a yield of 66.6 g as a colorless oil. The structure is confirmed by 1Hnmr and mass spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06800676B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-2fb68f64542c4872bd6ff6155d7c04a7 |
| Source note | uspto-grants-2004_10 |