HuagongsheHuagongshe Chemistry Print Report · For research reference only
4(2-Chloroallyl)benzaldehyde → 4(2-Chloroallyl)benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4(2-Chloroallyl)benzaldehyde | HCID 13243281 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4(2-Chloroallyl)benzyl alcohol | HCID 13243285 | — |
Reaction Steps
The aldehyde (0.25 g) of Example 1 in ether (5 ml) is added to lithium aluminum hydride (0.03 g) in ether (5 ml), and the mixture stirred at 20° for 1 hour. After successive dropwise additions of water (30 μl), 15% NaOH (30 μl) and water (90 μl), the resulting clear ether layer (+ washings) is evaporated to a residue of 4(2-chloroallyl)benzyl alcohol yield 0.22 g (86%) nD20 1.5504.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04827051 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-18d434c1f7874399a1be9583a9a099e5 |
| Source note | uspto-grants-1989_05 |