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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089400Generated: October 27, 2026

Phenolphthalein → HCID 53988615, compound

https://huagongshe.com/reaction/1089400

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 ether 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 numberUS04966732
Source datasetuspto-grants-1990_10
ORD IDord-ac4a4a4050aa4cacacb195fd5438a261
Source noteuspto-grants-1990_10