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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223670Generated: October 30, 2026

Isopropanol → HCID 20521627, compound

https://huagongshe.com/reaction/223670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantHCID 13073057HCID 13073057—
ReactantJones' reagentHCID 131709961—
Catalystchromium (VI) trioxideHCID 10219390—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
SolventDiethyl EtherHCID 3283—
ProductHCID 20521627HCID 20521627—

Reaction Steps

To a solution of 2.1 g of 8-bromo-6-octyn-1-ol (prepared as described hereafter) in 20 ml of acetone was added dropwise 7.7 ml of a Jones reagent (prepared by dissolving 6.5 g of chromium trioxide in 5.75 ml of conc. sulphuric acid diluted with water to a volume of 25 ml) at 2° to 5° C. over a period of 40 minutes. To it was addded 3 ml of isopropanol. The reaction mixture was diluted with diethyl ether, washed with water, a saturated aqueous solution of sodium chloride, dried over magnesium sulphate and concentrated under reduced pressure to give crude 8-bromo-6-octynoic acid. The crude product, thus obtained, was dissolved in 20 ml of diethyl ether, and diazomethane-etherate was added with cooling in an ice bath until the solution was coloured pale yellow. The reaction mixture was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixture of benzene and ethyl acetate (50:1) as eluent to give 1.583 g of the title compound having the following physical characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04355170
Source datasetuspto-grants-1982_10
ORD IDord-6ce426ad50c045fc897b1d569961a51e
Source noteuspto-grants-1982_10