Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | cis-1,3-Cyclohexanedicarboxylic anhydride | HCID 11367118 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10977233 | HCID 10977233 | — |
Reaction Steps
Anhydride 1 (7.71 g; 50 mmol) was combined with triethyl orthoformate (12.5 mL; 75 mmol; 1.5 equiv) and ethanol (50 mL). p-Toluenesulfonic acid (0.48 g; 2.5 mmol; 0.05 equiv) was added and the reaction mixture was heated overnight at 60° C. to completely consume 1. Solid sodium bicarbonate (0.5 g) was added and the solvent was removed at reduced pressure. The residue was dissolved in toluene (25 mL), washed with saturated aqueous NaHCO3 (5 mL), dried over Na2SO4, and concentrated to afford 11.42 g (99%) of cis-2b which was a single peak by GC analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06210956B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-103a8571befd42b9b33d9e2537247ea4 |
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| Source note | uspto-grants-2001_04 |
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