HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetophenone → 1-(3-Vinylphenyl)-1-phenylethyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | HCID 178436337 | HCID 178436337 | — |
| Product | 1-(3-Vinylphenyl)-1-phenylethyl alcohol | HCID 14423574 | — |
Reaction Steps
A method to use acetophenone (formula VIII) as a starting material is described. Acetophenone is reacted with a Grignard reagent of 3-vinylphenylmagnesium bromide (formula VII) to obtain 1-(3-vinylphenyl)-1-phenylethyl alcohol (formula V) (hereinafter referred to as "VPA"). The reaction product is then dehydrated in the presence of potassium hydrogensulfate to form 1-(3-vinylphenyl)-1-phenylethylene (formula I). This Grignard addition reaction is carried out at a temperature in the range of 0° to 100° C., preferably 20° to 80° C. The dehydration is carried out at 170° to 250° C., preferably 190° to 230° C., under a reduced pressure. The quantity of Grignard reagent is 1.0 to 1.2 equivalents relative to the acetophenone. ##STR7##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04822934 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-89c97cbc4e104cba83db2b8c69076ce2 |
| Source note | uspto-grants-1989_04 |