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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129532Generated: October 26, 2026

Cyclododecanecarboxaldehyde → 1-(3-Phenyl-1-propenyl)cyclododecane

https://huagongshe.com/reaction/129532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclododecanecarboxaldehydeHCID 78737—
ReactantPhenethyltriphenylphosphonium bromideHCID 10863251—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product1-(3-Phenyl-1-propenyl)cyclododecaneHCID 5447171688.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To 11.4 g (25.5 mmol) of phenylethyl triphenylphosphonium bromide in 50 mL of dry ether at 0° C. is added 10.2 mL (25.5 mmol) of 2.5M butyllithium. The suspension is stirred at 0° C. for 1 hour followed by the addition of 5.0 g (25.5 mmol) of cyclododecane carboxaldehyde. The mixture is stirred at room temperature for 3 hours after which time no starting material is evident by TLC. The reaction mixture is quenched with 1N HCl. The layers are separated and the aqueous layer is washed twice with ethyl ether. The combined organic layers are dried over a MgSO4 and the ether is evaporated. The residue is flash chromatographed on silica gel using hexanes to give 6.4 g of a colorless oil: NMR (CDCl3) δ 1.0-1.6 (m, 10H), 2.6 (m, 1H), 3.4 (d, 2H, J=8 Hz,), 5.3 (t, 1H, J=7 Hz), 5.45 (q, 1H, J=7 Hz), 7.2 ppm (m, 5

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468774
Source datasetuspto-grants-1995_11
ORD IDord-c1a0464607584b3bbe40ecd0acae5021
Source noteuspto-grants-1995_11