HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl Alcohol → HCID 58562927, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Bromo-2-fluorophenylacetyl chloride | HCID 58563097 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 58562927 | HCID 58562927 | — |
Reaction Steps
To a mixture of allyl alcohol (22.1 g, 380.5 mmol) and triethylamine (Et3N) (5.4 ml, 39 mmol) at 0° C. was added over 1 h crude (5-bromo-2-fluoro-phenyl) -acetyl chloride (intermediate B2A) (7.01 g, ca. 26 mmol). Then the reaction was stirred over 1 h from 0° C. to 23° C. The reaction mixture was diluted with ethyl acetate, washed with water, and the organic layer was dried over sodium sulfate. Removal of the solvent in vacuum left the title compound as a yellow oil (7.290 g, 103%), which was used without further purification. MS (ISP): m/z=280.1 [(M+NH4)+] and 282.1 [(M+2+NH4)+]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08673894B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-af763276818c432a9efd21062027d704 |
| Source note | uspto-grants-2014_03 |