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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761788Generated: October 27, 2026

4(2-Chloroallyl)benzaldehyde → 4(2-Chloroallyl)benzyl alcohol

https://huagongshe.com/reaction/1761788

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4(2-Chloroallyl)benzaldehydeHCID 13243281—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product4(2-Chloroallyl)benzyl alcoholHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04827051
Source datasetuspto-grants-1989_05
ORD IDord-18d434c1f7874399a1be9583a9a099e5
Source noteuspto-grants-1989_05