Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178475771 | HCID 178475771 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178477456 | HCID 178477456 | 37.6% |
Reaction Steps
To a 0° C. suspension of NaH (60% oil dispersion, 200 mg, 498 mmol) in THF (20 ml) was added ethanethiol (0.37 mL, 4.98 mmol). The resultant mixture was stirred for 10 min, cooled to -20° C., and compound 13 (1.9g, 3.83 mmol) was added. The solution was stirred further for 30 min at room temperature and concentrated. The residue was partitioned between ethyl acetate and pH 7.0 aqueous buffer. The organic phase was washed with brine, dried (Na2SO4), and concentrated. The residue was purified by silica gel chromatography (Et2O) to afford 718 mg (36%) of the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05175283 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-9a5c13ccf3ec4afa9b7027654fc39aec |
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| Source note | uspto-grants-1992_12 |
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