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 as a starting material will be described. Acetophenone is reacted with a Grignard reagent of m-vinylphenylmagnesium bromide to obtain 1-(3-vinylphenyl)-1-phenylethyl alcohol (formula IV) (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 III). 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., at a reduced pressure. The quantity of Grignard reagent is 1.0 to 1.2 equivalents relative to the acetophenone. ##STR9##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04937375 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-11b06fdfcfad4b1c9c00e41d0cc34e99 |
| Source note | uspto-grants-1990_06 |