HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzophenone → [4-Hydroxy-3-(prop-2-en-1-yl)phenyl](phenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzophenone | HCID 14347 | — |
| Reactant | 4-Allyloxybenzophenone | HCID 257910 | — |
| Product | [4-Hydroxy-3-(prop-2-en-1-yl)phenyl](phenyl)methanone | HCID 257912 | 47% |
Reaction Steps
4-hydroxybenzophenone (25 g) was converted to 4-allyloxybenzophenone (29.2 g, yellow solid) by the procedure of Example 23. Claisen rearrangement using that procedure gave 13.5 g (47%) of desired 3allyl-4-hydroxybenzophenone, the balance being recovered. Finally, acylation of 3-allyl-4-hydroxybenzophenone (5.9 G) according to general procedure of Example 1 produced 6.9 g (86%) of product as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04801610 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-64e158f082a94f37b08cdc212ec780e4 |
| Source note | uspto-grants-1989_01 |