HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 2-Chloro-1-phenylethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 2-Chloroacetophenone | HCID 10757 | — |
| Product | 2-Chloro-1-phenylethanol | HCID 92898 | 103.3% |
Reaction Steps
The procedure of Example 10 was followed using 0.773 g (5 mmol) of phenacyl chloride in lieu of benzaldehyde, to give 809 mg of 1-phenyl-2-chloroethanol as an oil. Conversion rate: 97.5%; yield 80.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06150567 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-0ec98237d0c54f00956e56f414521ff6 |
| Source note | uspto-grants-2000_11 |