Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224865Generated: October 30, 2026

Cyclohexanecarboxaldehyde → 1-Cyclohexylprop-2-en-1-ol

https://huagongshe.com/reaction/2224865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarboxaldehydeHCID 16275—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178418507HCID 178418507—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-Cyclohexylprop-2-en-1-olHCID 13819638%

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution of cyclohexanecarbaldehyde (4.79 mL, 39.8 mmol) in tetrahydrofuran (30 mL) was added dropwise to a solution of vinylmagnesium bromide (47.8 mL, 1M in tetrahydrofuran, 47.8 mmol) stirring at −20° C. The solution was stirred for 30 minutes at −20° C. at which time saturated ammonium chloride solution (75 mL) was added and the reaction was allowed to warm to 25° C. The solution was diluted with water and extracted three times with ethyl acetate. The ethyl acetate layers were combined and washed with brine, dried with sodium sulfate, filtered, and concentrated in vacuo. The residue was chromatographed on silica gel eluting with hexane, followed by 5% and 10% ethyl acetate in hexane to give the title compound (2.11 g, 38%). 1H NMR (300 MHz, CDCl3): δ ppm 1.40 m, 11 H) 3.85 (m, 1 H) 5.17 m, 2 H) 5.86 m, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378414B2
Source datasetuspto-grants-2008_05
ORD IDord-39ae4839f27f463e8b64b2c72968e046
Source noteuspto-grants-2008_05