HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 3-((Tert-butyldimethylsilyl)oxy)propanal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | 3-[(Tert-butyldimethylsilyl)oxy]propan-1-ol | HCID 4077791 | — |
| Catalyst | HCID 178419074 | HCID 178419074 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-((Tert-butyldimethylsilyl)oxy)propanal | HCID 3662392 | 69,024.297% |
Reaction Steps
Tetrapropylammonium perruthenate (0.18 g, 5.3 mmol) was added to a mixture of methylene chloride (20 mL) and acetonitrile (2 mL) containing 3-(tert-butyldimethylsilyloxy)-propanol (2 g, 0.01 mmol), N-methylmorpholine N-oxide (1.76 g) and 4 Å molecular sieves. The reaction mixture was stirred at RT overnight and then filtered through a pad of silica gel. The filtrate was concentrated under vacuo to afford 3-(tert-butyldimethylsilyloxy)-propionaldehyde (1.3 g, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07476676B2 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-81f3e1a46fd44b17a0bd3a3b063a5631 |
| Source note | uspto-grants-2009_01 |