HuagongsheHuagongshe Chemistry Print Report · For research reference only
Di(3-thienyl)methanol → Di(3-thienyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Di(3-thienyl)methanol | HCID 288490 | — |
| Reactant | HCID 178418287 | HCID 178418287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Di(3-thienyl)methanone | HCID 573773 | — |
Reaction Steps
To 2.1 gm (10.7 mmol) of Di-thiophen-3-yl-methanol in 50 mL of dichloromethane at room temperature was added 3.0 gm (13.9 mmol) of PCC. The reaction suspension was allowed to stir 2 hrs at room temperature. After 2 hrs, the reaction mixture was filtered and precipitates were washed with dichloromethane. The combined filtrates were concentrated. The concentrated sample was purified by flashy chromatography (hexane:ethyl acetate, from 11 to 18% ethyl acetate over 16 column volume) to obtain 1.83 gm (88.0%) of light yellow crystals; 1H NMR 500 MHz (CDCl3) δ 8.02 (d, 1H), 8.01 (d, 1H), 7.62 (d, 1H), 7.61 (d, 1H), 7.40 (d, 1H), 7.38 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07435822B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-75425183eb354c81a770cf9fa6f8368a |
| Source note | uspto-grants-2008_10 |