HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253583Generated: October 30, 2026
Dimethyl Sulfoxide → HCID 57786532, compound
https://huagongshe.com/reaction/253583
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 57786539 | HCID 57786539 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 57786532 | HCID 57786532 | 29% |
Reaction Steps
A 100 mL flask was charged with NaH (116 mg, 2.9 mmol) and Me3S+OI− (639 mg, 2.9 mmol) under N2. Dry DMSO (6 mL) was added. The mixture was stirred at rt for 1 h. A second 100 mL flask was charged with (S)-tert-butyl 1-oxo-3-(tetrahydro-2H-pyran-4-yl)propan-2-ylcarbamate (500 mg, 1.9 mmol) dissolved in THF (5 mL) under N2. The solution of NaH and Me3S+OI− was added through a syringe. The resulting mixture was stirred for 1 h. at rt. Brine was added and the mixture was extracted with EtOAc (3×10 mL). The organic phase was dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by chromatography to give tert-butyl (1S)-1-(oxiran-2-yl)-2-(tetrahydro-2H-pyran-4-yl)ethylcarbamate (150 mg, 29%). 1H NMR (CD3OD) δ 1.45 (s, 9H), 2.60 (b, 1 h), 2.75 (m, 1H), 3.0 (b, 1H), 3.35 (m, 2H), 4.0 (m, 3H), 4.30 (b, 1H), 5.30 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07872028B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-462ff61288424279aa1c3c301da6baf2 |
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| Source note | uspto-grants-2011_01 |
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