HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triacetoxyperiodinane → 4-Benzyloxymethyl-cyclohexanecarbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triacetoxyperiodinane | HCID 159087 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | ((1r,4r)-4-((Benzyloxy)methyl)cyclohexyl)methanol | HCID 22106763 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Benzyloxymethyl-cyclohexanecarbaldehyde | HCID 18667240 | 79% |
Reaction Steps
To a mixture of (4-benzyloxymethyl-cyclohexyl)-methanol (1.40 g, 6 mmol) in dichloromethane 28 mL is added Dess-Martin periodinate (2.53 g, 6 mmol) at 0° C., and the mixture is stirred for 0.5 hour while warming to room temperature. After addition of saturated aqueous NaHCO3, the mixture is extracted with EtOAc. The combined organic layer after dried over MgSO4 is concentrated to obtain 4-benzyloxymethyl-cyclohexanecarbaldehyde as clear oil (1.07 g, 79%) after purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08193349B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-2d2e21fa5c6b4d67a39a03d48b0dabf2 |
| Source note | uspto-grants-2012_06 |