Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfolane | HCID 31347 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | HCID 13605832 | HCID 13605832 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | Troglitazone | HCID 5591 | — |
Reaction Steps
A mixture of 9.6 g of ethyl 3-[4-(6-acetoxy-2,5,7,8-tetramethylchroman-2-ylmethoxy)phenyl]-2-chloropropionate (prepared as described in Preparation 51), 1.8 g of thiourea and 11 ml of sulfolane was heated for 3.5 hours at 120° C. under a nitrogen stream. 100 ml of ethylene glycol monomethyl ether and 70 ml of 10% w/v aqueous hydrochloric acid were then added to the reaction mixture, after which it was heated under reflux for 12 hours. The product was then purified as described in Example 27, to give the title compound. The melting point and nuclear magnetic resonance spectrum of this compound accorded with those of the compound obtained in Example 27(b).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05104888 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-1921ecf4562841c598ff796274bf7166 |
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| Source note | uspto-grants-1992_04 |
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