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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247183Generated: October 26, 2026

Phenolphthalein → HCID 53988615, compound

https://huagongshe.com/reaction/247183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolphthaleinHCID 4764—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Bromo-8-methylthiooctanoic acid ethyl esterHCID 54433491—
ReactantHCID 178418634HCID 178418634—
SolventWaterHCID 962—
ProductHCID 53988615HCID 5398861594%

Reaction Steps

8.6 grams (0.113 mole) of thioacetic acid in 20 ml of water-free ethanol were neutralized to phenolphthalein with 81 ml of 10% ethanolic potash solution (0.113 mole potassium hydroxide) and 29.7 grams (0.1 mole) of 6-bromo-8-methylthiooctanoic acid ethyl ester added. The mixture was heated at reflux for 6 hours in a nitrogen atmosphere and allowed to stand for 10 hours at room temperature. The precipitated potassium bromide was filtered off, the filtrate concentrated in a vacuum, the residue taken up in 300 ml of diethyl ether and filtered, the filtrate was washed twice, each time with 100 ml of water, dried with sodium sulfate and concentrated in a vacuum. There were obtained 26 grams (89% of theory) of crude 6-acetylthio-8-methylthiooctanoic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04705867
Source datasetuspto-grants-1987_11
ORD IDord-3bb1d4b26ea2489f8d8eeb05e663aaff
Source noteuspto-grants-1987_11