Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 4-Phenoxyphenol | HCID 13254 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (2S)-2-Methyloxirane | HCID 146262 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 9834706 | HCID 9834706 | — |
Reaction Steps
A solution of 4-phenoxyphenol (2.14 g, 11.5 mmol) in toluene (7 ml) was poured into an aqueous solution (3 ml) of sodium hydroxide (0.92 g, 23.0 mmol), and (S)-(-)propylene oxide (1.0 g, 17.24 mmol; a reagent manufactured by Aldrich; [α]D20 =-7.2° (CHCl3, c=1)) was added thereto while stirring. To the resultant mixture, tetra-n-butyl-ammonium bromide (185 mg) was added, and the mixture was stirred at room temperature for 12 hours, followed by addition of (S)-(-)-propylene oxide (1 g). After stirring at room temperature for 6 hours, the reaction mixture was vigorously stirred with addition of water (20 ml) and toluene (20 ml). The toluene layer was separated and washed with a 20 % aqueous sodium hydroxide solution and an aqueous sodium chloride solution in order and dried over magnesium sulfate. Removal of the solvent gave crude (S)-(+)-1-methyl-2-(4-phenoxyphenoxy)ethanol (2.35 g), which was further purified by silica gel column chromatography to give (S)-(+)-1-methyl-2-(4-phenoxyphenoxy)ethanol (1.97 g). [α]D23 =+14.0° (CHCl3, c=1). ee.: 72.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04970222 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-105b2cd6622c4caba86a3a7135fd0445 |
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| Source note | uspto-grants-1990_11 |
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