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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650646Generated: November 1, 2026

4-Dodecyloxy-2-chlorobenzoic acid → 4-Dodecyloxy-2-chlorobenzyl alcohol

https://huagongshe.com/reaction/1650646

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Dodecyloxy-2-chlorobenzoic acidHCID 19738841—
ReactantAluminium lithium hydrideHCID 21226445—
Product4-Dodecyloxy-2-chlorobenzyl alcoholHCID 54388926—

Reaction Steps

According to customary procedures, 4-dodecyloxy-2-chlorobenzoic acid synthesized in the same manner as described in Referential Example 15 was reduced with LiAlH4 to obtain 4-dodecyloxy-2-chlorobenzyl alcohol, and this compound was brominated with PBr3 to obtain 4-dodecyloxy-2-chlorobenzyl bromide. In the same manner as described in Referential Example 18, 2.0 g of the so-obtained compound was reacted with 1.0 g of 4-acetoxyphenol to obtain 4-dodecyloxy-2-chlorobenzyl(4-acetoxyphenyl) ether. Then, the acetyl group was removed by an equimolar amount of LiOH, whereby 0.9 g of 4-dodecyloxy-2-chlorobenzyl(4-hydroxyphenyl) ether was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925591
Source datasetuspto-grants-1990_05
ORD IDord-37132dbda6bf422f8118ed0261d86571
Source noteuspto-grants-1990_05