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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980393Generated: November 1, 2026

Ethanol → HCID 56623337, compound

https://huagongshe.com/reaction/1980393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantBicarbonate IonHCID 769—
ReactantEthyl orthoformateHCID 31214—
Reactant1-(4-isopropylphenyl)propan-1-oneHCID 3773435—
Catalystp-Toluenesulfonic acidHCID 6101—
CatalystTriethylamineHCID 8471—
ProductHCID 56623337HCID 5662333775.1%

Reaction Steps

48 ml of absolute ethanol and 1 g of p-toluenesulphonic acid are placed in a round flask which is fitted with a stirrer, thermometer, condenser and dropping funnel. Now, there are added dropwise within 30 minutes while stirring 181.5 g of p-isopropyl-propiophenone and subsequently within 1 hour 152.5 g of triethyl orthoformate. The temperature is held at 30° C. by external cooling. The mixture is subsequently stirred for a further 22 hours at 20°-25° C. The mixture is then adjusted to pH 8 with 5 g of triethylamine and thereupon poured into 50 ml of 5% bicarbonate solution and 80 g of ice. The aqueous phase is separated and extracted with ether. The combined organic phases are washed with 5% bicarbonate solution and, after the addition of 0.3 g of sodium carbonate, the solvent is removed by evaporation under a vacuum and the residue is distilled over a 15 cm column. There are obtained 193.6 g of p-isopropyl-propiophenone diethyl ketal (yield: 75.1% of theory). B.p.=66° C./0.05 mmHg; nD20 =1,4778; d420 =0,9305.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04508925
Source datasetuspto-grants-1985_04
ORD IDord-d146eb24809640d6a297a16a6f299d3d
Source noteuspto-grants-1985_04