Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 10824826 | HCID 10824826 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15870214 | HCID 15870214 | 82% |
Reaction Steps
To a suspension of sodium borohydride (1.78 g) in tetrahydrofuran (70 ml)is added dimethylsulfide (2.8 ml) at room temperature, and thereto is added dropwise a solution of boron trifluoride·ether complex (6.3 ml) in tetrahydrofuran (10 ml) at room temperature, and the mixture is stirred for 30 minutes. To the mixture is added (3R)-3-benzylthio-3-carboxypropionic acid methyl ester (10 g) at room temperature, and the mixture is stirred for 1.5 hour. After the reaction is completed, to the reaction solution are added successively 2N aqueous sodium hydroxide solution (16 ml), 30% aqueous hydrogen peroxide solution (11 ml), and then further added a saturated aqueous sodium chloride solution. The mixture is extracted with chloroform, and the extract is dried, concentrated under reduced pressure, and the residue is purified by silica gel column chromatography (solvent; n-hexane:ethyl acetate=2:1) to give (3R)-3-benzylthio-4-hydroxybutyric acid methyl ester (7.75 g) as an oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05629419 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-a8e4e6fcd8f14bcc9cedcf551546834c |
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| Source note | uspto-grants-1997_05 |
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