HuagongsheHuagongshe Chemistry Print Report · For research reference only
4(Z-3-chloroallyl)benzaldehyde → 4(Z-3-chloroallyl)benzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4(Z-3-chloroallyl)benzaldehyde | HCID 13243338 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4(Z-3-chloroallyl)benzyl alcohol | HCID 13243348 | — |
Reaction Steps
The aldehyde (0.22 g) of Example 1 in ether (5 ml) is added to lithium aluminium hydride (0.08 g) in ether (5 ml), and the mixture stirred at 20° for 1 hour. After successive dropwise additions of water (80 l), 15% NaOH (80 l) and water (240 l), the resulting clear ether layer (+ washings) is evaporated to a residue of 4(Z-3-chloroallyl)benzyl alcohol yield 0.19 g (86%) nD20 1.5529.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04847438 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-b06ab0339a0c49c98a49f6a1670d1458 |
| Source note | uspto-grants-1989_07 |