HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cornforth reagent → Spiro(2.5)octane-6-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cornforth reagent | HCID 2724130 | — |
| Reactant | (Spiro(2.5)octan-6-yl)methanol | HCID 53487089 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Spiro(2.5)octane-6-carbaldehyde | HCID 86598198 | — |
Reaction Steps
Spiro[2.5]oct-6-yl-methanol (2.57 g, 18.3 mmol, 1.0 eq.) was dissolved in CH2Cl2 (30 mL) and placed in a ice-water bath at 0° C. Pyridinium dichromate (PCC) (7.9 g, 36.6 mmol, 2.0 eq.) was added and the reaction warmed to room temperature for 4 hours with stirring. The crude reaction was filtered through a Celite pad and washed with CH2Cl2 and evaporated. The crude material was dissolved in diethyl ether and filtered through Celite, washing with diethyl ether several times. Evaporated solvent to provide Spiro[2.5]octane-6-carbaldehyde as a brown oil (2.98 g, quantitative) that was used directly. 1H NMR (CHCl3, 400 MHz) δ 0.17-0.27 (m, 4H), 0.88-0.91 (m, 2H), 1.09-1.25 (m, 2H), 1.52-1.54 (m, 2H), 1.69-1.75 (m, 3H), 9.44 (d, 1H, J=1.2 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07732449B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-c30f4ecb7f5a47108df6f7c307355618 |
| Source note | uspto-grants-2010_06 |