HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-(4-Methyl-1-oxo-1,3-dihydroisobenzofuran-5-yl)acetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | 4-methyl-5-prop-2-en-1-yl-2-benzofuran-1(3H)-one | HCID 66646536 | — |
| Product | 2-(4-Methyl-1-oxo-1,3-dihydroisobenzofuran-5-yl)acetaldehyde | HCID 77231260 | — |
Reaction Steps
A solution of 4-methyl-5-prop-2-en-1-yl-2-benzofuran-1(3H)-one (220 mg, 1.2 mmol) in MeOH (20 mL) was cooled to −78° C. To this solution was bubbled ozone until the reaction turned blue. Nitrogen was bubbled through the reaction to drive off excess ozone, followed by addition of DMS (0.870 mL, 11.7 mmol). The reaction was allowed to warm up to RT. The solvents were removed under reduced pressure. The crude product was purified by flash chromatography to afford (4-methyl-1-oxo-1,3-dihydro-2-benzofuran-5-yl)acetaldehyde. 1H-NMR (500 MHz, CDCl3) δ ppm 9.78 (s, 1H), 7.75 (d, J=7.5 Hz, 1H), 7.34 (d, J=7.5 Hz, 1H), 5.27 (s, 2H), 3.90 (s, 2H), 2.23 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09056859B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-5b3392d0b99e40fabcc63469cc2062dc |
| Source note | uspto-grants-2015_06 |