HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 3-Chloro-1-phenyl-3-buten-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2,3-Dichloropropene | HCID 6565 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Chloro-1-phenyl-3-buten-1-ol | HCID 14663678 | 95.2% |
Reaction Steps
125.40 Grams of 2,3-dichloro-1-propene were added dropwise to a mixture of 60.00 g of benzaldehyde, 180 g of toluene, 240 g of 5% acetic acid and 73.88 g of zinc powder at 45° C., and then the mixture was allowed to react at the same temperature for 3 hours. After the reaction was completed zinc-derived insolubles were filtered off, and the resultant filtrate was subjected to separation. The organic phase was washed with a 7% sodium carbonate aqueous solution and dried over sodium sulfate. The desiccant was filtered off, and then the toluene was distilled off under reduced pressure to give 98.23 g of 2-chloroallylphenylcarbinol. The results were as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05258529 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-844ea650780e43d795ec8dfa4a3ab69f |
| Source note | uspto-grants-1993_11 |