HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 7-[(Trifluoromethylsulfonyl)oxy]-3-phenylmethyl-benzopyran-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 7-Trifluoromethylsulfonyloxy-benzopyran-4-one | HCID 21955570 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-[(Trifluoromethylsulfonyl)oxy]-3-phenylmethyl-benzopyran-4-one | HCID 15347250 | 75% |
Reaction Steps
To a stirred solution of the product of Step C (27 g, 91.2 mmole) in 183 mL of methanol was added benzaldehyde (11.1 mL, 109 mmole) followed by pyrrolidine (9.1 mL, 109 mmole). The mixture was stirred at room temperature overnight, cooled to 0° C. and filtered. The solid was washed once with 50 mL of ice-cold methanol and then dried in vacuo; 35.2 g, (75% yield) of the title product was recovered. M.P. 133°-135° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05684046 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-9af9f26bd9e04f34bcef218a1ac41329 |
| Source note | uspto-grants-1997_11 |