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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256736Generated: October 27, 2026

Benzaldehyde → 3-Chloro-1-phenyl-3-buten-1-ol

https://huagongshe.com/reaction/256736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantTolueneHCID 1140—
Reactant2,3-DichloropropeneHCID 6565—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product3-Chloro-1-phenyl-3-buten-1-olHCID 1466367895.2%

Reaction Steps

125.40 Grams of 2,3-dichloro-1-propene were added dropwise to a mixture of 60.00 g of benzaldehyde, 180 g of toluene, 240 g of 5% acetic acid and 73.88 g of zinc powder at 45° C., and then the mixture was allowed to react at the same temperature for 3 hours. After the reaction was completed zinc-derived insolubles were filtered off, and the resultant filtrate was subjected to separation. The organic phase was washed with a 7% sodium carbonate aqueous solution and dried over sodium sulfate. The desiccant was filtered off, and then the toluene was distilled off under reduced pressure to give 98.23 g of 2-chloroallylphenylcarbinol. The results were as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258529
Source datasetuspto-grants-1993_11
ORD IDord-844ea650780e43d795ec8dfa4a3ab69f
Source noteuspto-grants-1993_11