HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → (2S)-4-{[tert-butyl(diphenyl)silyl]oxy}butan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Reactant | (+)-1,3-Butanediol | HCID 446973 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | (2S)-4-{[tert-butyl(diphenyl)silyl]oxy}butan-2-ol | HCID 58005224 | — |
Reaction Steps
Under ice cooling, to a dichloromethane solution (20.0 ml) of (S)-1,3-butanediol (519 mg) were added triethylamine (1.04 ml) and tert-butylchlorodiphenylsilane (1.63 ml), followed by stirring at room temperature overnight. The reaction solution was poured into a saturated aqueous ammonium chloride solution, and extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography to afford (2S)-4-{[tert-butyl(diphenyl)silyl]oxy}butan-2-ol (1.69 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08729095B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-25728101a12f47a6b6ac19b9099b809e |
| Source note | uspto-grants-2014_05 |