Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Naphthol | HCID 7005 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (S)-(-)-3-Chloro-1-phenyl-1-propanol | HCID 2777894 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Dapoxetine Impurity 13 | HCID 54389814 | 54% |
Reaction Steps
To a mixture of 8 ml of DMF and 0.44 g of 60% sodium hydride in mineral oil at 5° C. in an ice bath was added dropwise a solution of 1.44 g of 1-naphthol in 8 ml of DMF. The reaction mixture was stirred at 5° C. for two hours and a solution of 1.71 g of (S)-(-)-3-chloro-1-phenyl-1-propanol in 5 ml of DMF was added. After stirring overnight at room temperature, the reaction mixture was poured into 150 ml of water and extracted with ethyl acetate (3×50 ml). The combined extracts were combined and washed with water and 1N sodium hydroxide solution and dried over sodium sulfate. Yield: 2.56 g (92%). The crude product can be recrystallized from 95:5 hexane/ethyl acetate to give 1.5 g (54%) of purified (S)-(+)-3-(1-naphthalenyloxy)-1-phenyl-1-propanol, mp 76°-78° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05292962 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-42bd86c252904e7898392f8f6a2211c5 |
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| Source note | uspto-grants-1994_03 |
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