HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzaldehyde → 4'-(3-Phenylpropoxy)acetophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | 4'-Hydroxyacetophenone | HCID 7469 | — |
| Reactant | 2'-Hydroxyacetophenone | HCID 8375 | — |
| Product | 4'-(3-Phenylpropoxy)acetophenone | HCID 19596236 | — |
| Product | o-(3-Phenylpropoxy)acetophenone | HCID 21422420 | — |
| Product | 1-[3-(3-Phenylpropoxy)phenyl]ethan-1-one | HCID 21422440 | — |
Reaction Steps
Following essentially the same procedure, but substituting o-hydroxyacetophenone, m-hydroxyacetophenone, and p-hydroxyacetophenone for the p-hydroxybenzaldehyde above, results in the formation of o-(3-phenylpropoxy)acetophenone (b.p. 173°-8° C. at 0.1 mm), m-(3-phenylpropoxy)acetophenone (b.p. 199°-201° C. at 0.2 mm) and p-(3-phenylpropoxy) acetophenone (m.p. 80°-1° C.), respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04038412 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-f0b763cbef82402b82ff1a570d10df9a |
| Source note | uspto-grants-1977_07 |