HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → Stilbene oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 1-Methoxy-4-(methylthio)benzene | HCID 15885 | — |
| Reactant | Benzene, (diazomethyl)- | HCID 136601 | — |
| Catalyst | Acetic acid, rhodium(2+) salt | HCID 21674 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Stilbene oxide | HCID 28649 | — |
Reaction Steps
To a mixture of rhodium (II) acetate (0.0021 g), dichloromethane (4 ml) and benzaldehyde (0.051 ml) was added 1-methoxy-4-methylthiobenzene (0.0036 ml). To this mixture was added, with stirring, a solution of phenyldiazomethane (1 mmol in tert-butylmethyl ether (8 ml)) over 19 hours. The reaction mixture was stirred or a further 5 hours after which the mixture was allowed to stand at room temperature for 2 days. The solvent was removed in vacuo and the residue chromatographed on silica using dichloromethane:hexane 2:3 as eluant. The title compound was obtained as a colourless oil (0.0713 g, 22.6% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05703246 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-0dbe1c655d8e40b7be2f8453fee14b0f |
| Source note | uspto-grants-1997_12 |