Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aspirin | HCID 2244 | — |
| Reactant | Solketal | HCID 7528 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15341562 | HCID 15341562 | — |
Reaction Steps
The solution from 2-acetoxybenzoic acid (10.0 g, 55.5 mmol) in dichloromethane (200 ml) is treated with triethylamine (7.7 ml, 55.5 mmol), cooled to 0° C., treated dropwise with ethyl chloroformate (5.3 ml, 55.5 mmol), stirred at 0° C. for 1 h and filtered. The filtrate is added at room temperature to a solution of (±)-2,2-dimethyl-4-hydroxymethyl-1,3-dioxolane (7.33 g, 55.5 mmol) and triethylamine (50 ml) in dichloromethane (100 ml). After 4 h, water (50 ml) is added and the mixture is stirred. The organic phase is washed with dilute hydrochloric acid, saturated aqueous sodium hydrogencarbonate solution and water, dried over magnesium sulphate and concentrated. The residue is purified by column chromatography on silica gel 60 (hexane/ethyl acetate =15/1). Yield: 8.4 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05859053 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-8457430ff45f4028b760b543f0a4ee8a |
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| Source note | uspto-grants-1999_01 |
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