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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975615Generated: October 28, 2026

Tetrahydrofuran → 4-(4-Bromophenyl)cyclohexane-1-carbaldehyde

https://huagongshe.com/reaction/1975615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-Bromo-4-[4-(methoxymethylidene)cyclohexyl]benzeneHCID 19097914—
SolventWaterHCID 962—
Product4-(4-Bromophenyl)cyclohexane-1-carbaldehydeHCID 1909790195.1%

Reaction Steps

A mixture of 10.4 g of 1-bromo-4-[4-(methoxymethyli-dene)cyclohexyl]benzene and 100 ml of tetrahydrofuran/2N hydrochloric acid (vol. 4:1) was heated to reflux for 30 minutes in a round flask. Subsequently, the reaction mixture was poured into 100 ml of water and extracted three times with 100 ml of diethyl ether each time. The organic phases were washed with 100 ml of water, dried over magnesium sulphate and concentrated. There were obtained 9.4 g of 4-(4-bromophenyl)cyclohexanecarboxaldehyde as white crystals; trans/cis ratio about 5:3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05288428
Source datasetuspto-grants-1994_02
ORD IDord-1ccd38fd5d124569bac9e683f3bf82a6
Source noteuspto-grants-1994_02