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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099477Generated: October 31, 2026

Benzene → 1-Allylcyclohexanecarbaldehyde

https://huagongshe.com/reaction/1099477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantAllyl AlcoholHCID 7858—
ReactantCyclohexanecarboxaldehydeHCID 16275—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
SolventWaterHCID 962—
Product1-AllylcyclohexanecarbaldehydeHCID 1180496378%

Reaction Steps

A mixture of cyclohexanecarboxaldehyde ((10 mL, 0.825 mol), allyl alcohol (60 mL, 98% purity, 0.882 mol), benzene (15 mL), and p-toluenesulfonic acid monohydrate (0.120 g, 0.63 mmol) was heated from 130° C. to 180° C. in an oil bath, under a Vigreaux distillation column, topped by a Dean-Stark trap. After 15 hour no more water was added over the 15 mL collected in the trap, and the reaction was judged completed. Subsequent distillation of the reaction crude gave 98 g (78% yield) of 1-allyl-cyclohexanecarboxaldehyde as a colourless liquid (b.p. 69-71° C./5 mm Hg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143443B2
Source datasetuspto-grants-2012_03
ORD IDord-a3eef575d734412ca41ad26a11cddb98
Source noteuspto-grants-2012_03