Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2,2-Dimethoxypropane | HCID 6495 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | HCID 53675379 | HCID 53675379 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19761822 | HCID 19761822 | 73.3% |
Reaction Steps
To a solution of 1-methyl 6-ethyl 2,4-dihydroxyadipate (1.5 g, 6.81 mmol) in methylene chloride (60 ml), dimethoxypropane (1.672 ml, 78 mmol) and pyridinium p-toluenesulfonate (251 mg, 1 mmol) were added and stirred under reflux conditions for one hour, followed by further stirring at 50° C. for one hour while azeotropically removing methanol with methylene chloride. Then, after adding methylene chloride (60 ml), the mixture was again stirred at 50° C. for one hour to remove methylene chloride (50 ml). To the residue, water was added, and the mixture was extracted with methylene chloride. The organic layers were combined, dried over sodium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (hexane:acetone=5:1) to give pure 2-methoxycarbonyl-4-ethoxycarbonylmethyl-6,6-dimethyl-1,5-dioxane (1.29 g, 4.99 mmol). Yield, 73 %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05214197 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-727f0fc43dde46ddbc63bc7e76c0c6af |
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| Source note | uspto-grants-1993_05 |
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