Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 66662149 | HCID 66662149 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 66661680 | HCID 66661680 | — |
Reaction Steps
To a mixture of 1-{4-[cyclopentyl(fluoro)methyl]phenyl}cyclopropanecarbonitrile (600.0 mg, 0.002466 mol) and 19.4 M of sodium hydroxide in water (0.51 mL) was added 1,2-ethanediol (5 mL, 0.09 mol), and the mixture was refluxed at 100° C. overnight. After cooling down to rt, the reaction mixture was poured into water and extracted with ether. The aqueous phase then was acidified with HCl and extract with ether. Then the organic phase was washed with brine, dryed over MgSO4, and concentrated to afford the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09126927B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-682124e0794741de915fe04894102677 |
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| Source note | uspto-grants-2015_09 |
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