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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383791Generated: October 26, 2026

Salbutamol → Salbutamol glycodeoxycholate

https://huagongshe.com/reaction/1383791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalbutamolHCID 2083—
ReactantEthyl AcetateHCID 8857—
ReactantGlycodeoxycholic AcidHCID 3035026—
SolventEthanolHCID 702—
ProductSalbutamol glycodeoxycholateHCID 131722754105.9%

Reaction Steps

Salbutamol base (1.2007 g; 5.02 mmol) was dissolved in ethanol (100 mL) with vigorous stirring. Glycodeoxycholic acid (2.4601 g; water content: 4.25% w/w; 5.25 mmol˜5% molar excess) was added and dissolved with stirring. A clear, colourless solution was obtained. The ethanol was removed by vacuum rotary-evaporation to give a viscous, yellow residue. Ethyl acetate (200 mL) was added to the residue and the mixture heated in a water bath with constant agitation. As the yellow residue dissolved, a white precipitate formed. Agitation was continued until the yellow residue disappeared. The ethyl acetate solution was cooled in an ice bath. The precipitate was isolated by vacuum filtration and dried in a vacuum oven at 40° C. for 20 hours to give salbutamol glycodeoxycholate (3.662 g; water content; 4.95% w/w; % yield; 97.9%). Analysis by differential scanning calorimetry from 50 to 200° C. gave no significant thermal event. Slow decomposition was evident after 110° C. A saturated aqueous solution gave a pH of 6.12. The aqueous solubility was greater than 8.35 mg/mL. The theoretical percentage of salbutamol base in the salbutamol glycodeoxycholate 34.74%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255502B1
Source datasetuspto-grants-2001_07
ORD IDord-2df3eac4f00b4382adc03e49033db230
Source noteuspto-grants-2001_07