HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 57225501, compound → HCID 57021050, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 57225501 | HCID 57225501 | — |
| Reactant | HCID 178490222 | HCID 178490222 | — |
| Catalyst | Copper bromide (CuBr2) | HCID 24611 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57021050 | HCID 57021050 | 105.4% |
Reaction Steps
To a solution of (1R,2S)-1-(4,5-diphenyloxazol-2-yl)-1,2-epoxycyclohexane (20 g) and copper bromide (3.0 g) in tetrahydrofuran (400 ml) was dropwise added a solution of 3-methoxybenzylmagnesium chloride [prepared from 3-methoxybenzylchloride (50 g) and Mg (9.2 g)] in tetrahydrofuran (500 ml) at −78° C. under N2. The mixture was stirred for 2 hours at the room temperature and partitioned between EtoAc and water. The organic layer was washed with 1N-hydrochloric acid, water, saturated sodium hydrogencarbonate and brine. The dried solvent was evaporated in vacuo and the residue was purified by chromatography on silica gel to give (1R,2S)-1-(4,5-diphenyloxazol-2-yl)-1-hydroxy-2-(3-methoxybenzyl)cyclohexane (29.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06437146B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-4360e0ca6bfc4700be171a6f8d383de3 |
| Source note | uspto-grants-2002_08 |