HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 2-Hydroxy-1-phenyl-1-propanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 2-Bromopropiophenone | HCID 16452 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Hydroxy-1-phenyl-1-propanone | HCID 101121 | 98% |
Reaction Steps
There was added 10.08 parts of sodium bicarbonate and about 60 parts of water to a mixture of 21.3 parts of α-bromopropiophenone, 6.8 parts of sodium formate and about 90 parts of acetonitrile. The resulting mixture was stirred vigorously for 48 hours at 65° C. during which time carbon dioxide evolved. After cooling, the acetonitrile solution was separated from the aqueous layer and evaporated to dryness. The residue was dissolved into chloroform which was extracted once with water, dried over sodium sulfate, and evaporated to produce analytically pure (>98%) α-hydroxypropiophenone. The yield of this isolated product was 77.1%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04158094 |
| Source dataset | uspto-grants-1979_06 |
| ORD ID | ord-d494b997ee4a4071bf5ea7d6d61be2ab |
| Source note | uspto-grants-1979_06 |