HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxygen → HCID 21940165, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 21940186 | HCID 21940186 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21940165 | HCID 21940165 | — |
Reaction Steps
5-(3-acetoxyphenyl)-4-(13-ethoxycarbonyl-1,1-dimethyl-3-oxatridecan-1-yl)-3,3-dimethyl-2,3-dihydrofuran (compound (24)) (57.8 mg, 0.112 mmol) and TPP (0.6 mg) were added to dichloromethane (6 mL), and the mixture was irradiated with visible light by a 940 W sodium lamp in an oxygen atmosphere at 0° C. for 30 minutes. The reaction mixture was concentrated, and the concentrate was put into a silica gel column and developed with a mixed solvent of hexane and ethyl acetate (10:1 to 5:1), whereby 1-(3-acetoxyphenyl)-5-(13-ethoxycarbonyl-1,1-dimethyl-3-oxatridecan-1-yl)-4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptane (compound (25)) was obtained as a colorless oil in an amount of 46 mg in a yield of 75.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115757B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-68fe41d1afcf417dbbc940b57e3a0dae |
| Source note | uspto-grants-2006_10 |