Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(3-Chlorophenyl)ethanone | HCID 14933 | — |
| Reactant | Glyoxylic acid, monohydrate | HCID 15620607 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | 191014-74-1 | HCID 10081862 | 39.2% |
Reaction Steps
A stirred mixture of 3'-Chloroacetophenone (15 mL, 97 mmol) and glyoxylic acid monohydrate (9 g, 97 mmol) was heated at 130° C. under reduced pressure (1,5 mmHg), over 8 hours. During this time the reduced pressure was maintained in order to remove the water formed during the reaction. After cooling, the crude reaction product was taken up in aqueous 10% potassium carbonate solution (100 mL) and the resulting solution was washed with diethyl ether (3×30 mL), the alkaline aqueous layer was cooled at 0° C. and then cautiously acidified with 6N HCl. The resulting suspension was extracted with ethyl acetate (3×50 mL), the collected organic extracts were washed with brine and dried (Na2SO4). Concentration of the solvent in vacuo afforded a yellow solid (8 g) which was chromatographed (SiO2 ;CH2Cl2 /MeOH 98:2) to provide the pure acid (6 g, 30%), lightly yellow solid melting at 158-59° C. (diisopropyl ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06048896 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-3771ff92a6f64d87be275cef67f490d9 |
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| Source note | uspto-grants-2000_04 |
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