HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091372Generated: November 1, 2026
Chlorotrimethylsilane → HCID 66594479, compound
https://huagongshe.com/reaction/1091372
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | HCID 86630238 | HCID 86630238 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66594479 | HCID 66594479 | 67% |
Reaction Steps
Chlorotrimethylsilane (96 g, 884 mmol) was added to a solution of lithium borohydride (9.6 g, 441 mmol) in tetrahydrofuran (500 ml) and the solution was stirred for one hour at room temperature. A solution of 4-((2S)-4-benzyl-5-oxo-morpholin-2-yl)phenyl methanesulfonate (79.8 g, 221 mmol) in tetrahydrofuran (200 ml) was added to the solution and stirred at room temperature for one hour. After careful addition of methanol (60 ml) under ice-cooling, the solvent was removed under reduced pressure. Potassium hydroxide (145 g, 2.2 mol) was added to a solution of the residue in ethanol (300 ml) and water (300 ml) and the solution was stirred at 80° C. for 2 hours. The solvents were removed under reduced pressure and the residue was extracted with ethyl acetate and dried over anhydrous magnesium sulfate. Removal of the solvent yielded (2S)-4-benzyl-2-(4-hydroxyphenyl)morpholine (39.8 g, 67%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129377B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-71c0beb14fbc45979571c175e45b85ae |
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| Source note | uspto-grants-2012_03 |
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