Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231670Generated: October 27, 2026

4(Z-3-chloroallyl)benzaldehyde → 4(Z-3-chloroallyl)benzyl alcohol

https://huagongshe.com/reaction/231670

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4(Z-3-chloroallyl)benzaldehydeHCID 13243338—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product4(Z-3-chloroallyl)benzyl alcoholHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04847438
Source datasetuspto-grants-1989_07
ORD IDord-b06ab0339a0c49c98a49f6a1670d1458
Source noteuspto-grants-1989_07