Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 21312955 | HCID 21312955 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 53700903 | HCID 53700903 | 62% |
Reaction Steps
8 g (56.3 mmol) of 5-methyl-1,2,4-oxadiazol-3-yl-acetic acid were suspended in 8 g (80 mmol) of re-distilled, dry cyclohexanol and 8 g (52.2 mmol) of phosphorous oxychloride were added dropwise under anhydrous conditions over about 7 minutes to the mixture. During the addition, the mixture was heated on a steam bath and heating was continued for 45 minutes. After the reaction mixture had cooled to room temperature, 75 ml of ice-water and 50 ml of diethyl ether were added and the mixture was stirred until a clear two-layer system was obtained. The flask was placed in an ice-salt bath and solid potassium hydroxide was added until a pH of 10.5 was reached. The layers were separated and the aqueous layer was extracted three times with 40 ml portions of diethyl ether. The four ethereal extracts were combined, washed once with a small volume of ice-water and subsequently concentrated in vacuo. The 10 g of residue was distilled in vacuo to obtain 7.9 g (62% yield) of cyclohexyl 5-methyl-1,2,4-oxadiazol-3-yl-acetate with a b.p. of 120°-121° C. at 0.9-1.0 mm and a refractive index nD25 =1.4715.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04160829 |
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| Source dataset | uspto-grants-1979_07 |
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| ORD ID | ord-1697d700571d481abd44495b02aa18c3 |
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| Source note | uspto-grants-1979_07 |
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