HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl morpholine oxide → 2-[(1R,2S,3R)-2,3-dihydroxycyclohexyl]-1H-isoindole-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | Propan-2-one--water (1/1) | HCID 18366337 | — |
| Reactant | 2-[(1R)-cyclohex-2-en-1-yl]-1H-isoindole-1,3(2H)-dione | HCID 58369653 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Product | 2-[(1R,2S,3R)-2,3-dihydroxycyclohexyl]-1H-isoindole-1,3(2H)-dione | HCID 58369651 | 95% |
Reaction Steps
To a suspension of 2-[(1R)-cyclohex-2-en-1-yl]-1H-isoindole-1,3(2H)-dione (18) (19.9 mmol, 4.53 g) and 4-methylmorpholine-N-oxide (60 mmol, 7.01 g) in acetone/water (4:1, 62.5 mL), osmium tetroxide (0.2 mmol, 50 mg) was added. The reaction was stirred for 4 h. The mixture was concentrated and saturated sodium sulfite (40 mL) was added. It was then promptly extracted with EtOAc three times. The combined organic layers were washed with water and brine, dried over MgSO4 and concentrated to give the crude product as a white solid (4.94 g, 95% yield). Chiral HPLC [8.53 min]. Analytical data matched published data (Donohoe, J. T.; et al., J. Org. Chem., 2002, 67, 7946-7956)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889719B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-0d962995f39542ec8daa9ecf265cd1ae |
| Source note | uspto-grants-2014_11 |