HuagongsheHuagongshe Chemistry Print Report · For research reference only
3'-Bromoacetophenone → HCID 60795076, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3'-Bromoacetophenone | HCID 16502 | — |
| Reactant | HCID 178425413 | HCID 178425413 | — |
| Product | HCID 60795076 | HCID 60795076 | — |
Reaction Steps
In an analogous reaction sequence to that described for Building Block C, the reaction of 3-methyl phenylmagnesium bromide with 3-bromoacetophenone yielded the 1-(3-bromo-phenyl)-1-m-tolyl-ethanol which was used as crude material in the following elimination reaction with a catalytic amount of p-toluenesulfonic acid to yield the title compound (yield: 66% of theory) as a colourless oil. TLC: Rf: 0.83 (silica gel; heptane:ethyl acetate=4:1, UV, 254 nm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07989449B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-82d1143cca7048d79aeb7de18b0bf2d4 |
| Source note | uspto-grants-2011_08 |