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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210870Generated: November 1, 2026

12-Bromo-1-dodecanol → 12-Bromododecanal

https://huagongshe.com/reaction/2210870

Reaction equation

Participants

RoleNameHCIDCharge
Reactant12-Bromo-1-dodecanolHCID 137895—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
Product12-BromododecanalHCID 1178033588.7%

Reaction Steps

To 12-bromododecanol (5 g) dissolved in methylene chloride (30 ml) were added Celite (5.0 g) and pyridinium chlorochromate (5.2 g), and the mixture was stirred at room temperature for 12 hours. Then, .the reaction mixture was filtered and subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (30:1) to give 12-bromododecanal (4.4 g). To 12-bromododecanal (4.4 g) dissolved in methylene chloride (50 ml) was added (carbomethoxymethylene)triphenylphosphorane (6.75 g), and the mixture was stirred for 4 hours. Then, the reaction mixture was concentrated, and the residue thus obtained was subjected to chromatography on a silica gel column with an eluent system of n-hexane-ethyl acetate (30:1) to give the methyl ester of 14-bromo-2-tetradecenoic acid (4.91 g). The product was dissolved in acetonitrile (30 ml), and 1M tetra-n-butylammonium chloride in THF (27 ml) and potassium fluoride (7.6 g) were added. The mixture was heated under reflux for 12 hours. The reaction mixture was concentrated and subjected to chromatography on a silica gel column with an eluent system of n-hexaneethylacetate 100:1 to give the methyl ester of 14-fluoro-3-tetradecenoic acid (3.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05461036
Source datasetuspto-grants-1995_10
ORD IDord-83e460eddb984e3f9a6efa8bab29a793
Source noteuspto-grants-1995_10