HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462568Generated: October 30, 2026
Propylene Glycol → 1,3-Dioxolane, 4-methyl-2-[2-(methylthio)ethyl]-
https://huagongshe.com/reaction/462568
Participants
| Role | Name | HCID | Charge |
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| Reactant | Propylene Glycol | HCID 1030 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Butanthial | HCID 12463483 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,3-Dioxolane, 4-methyl-2-[2-(methylthio)ethyl]- | HCID 100927 | — |
Reaction Steps
Into a 100 ml reaction flask equipped with spin bar, reflux condenser, heating mantle and hot plate with magnetic stirring apparatus is placed 5 ml cyclohexane, 0.2 grams para-toluenesulfonic acid and 3.8 grams (0.05 moles) of 1,2-propanediol. Over a period of 8 hours, 3-methylthiopropionaldehyde is added to the reaction mass. The reaction mass is then heated to reflux and during refluxing water of formation is removed. The refluxing continues for a period of 7 hours. At the end of the 7 hour period, the reaction mass is transferred to a separatory funnel and washed with one 50 ml portion of saturated aqueous sodium chloride solution and then dried over anhydrous sodium sulfate, filtered and distilled on a Microvigreux column yielding the following fractions:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04515966 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-dee058d289184193a15c03ac9d87f9af |
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| Source note | uspto-grants-1985_05 |
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