HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → HCID 22630547, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 22630555 | HCID 22630555 | — |
| Product | HCID 22630547 | HCID 22630547 | 53% |
Reaction Steps
In a single-neck flask, 1.2 g (2.8×10−3 mol) of 2-(N-carbazolyl)-5-(2′-ethylhexyloxy)-1,4-bis(hydroxymethyl) benzene synthesized in the above step (7) was dissolved in 250 ml of absolute chloroform, and 0.26 ml (2.8×10−3 mol) of POCl3 and 0.21 ml (2.8×10−3 mol) of DMF stirred in 150 ml of chloroform were slowly added. The reaction was left to stand at room temperature for 12 hours, and then the reaction solution was washed several times with water, and water in the organic layer was removed with MgSO4 and vacuum-distilled. The oil so produced was purified by column chromatography using a hexane developing solution. Yield: 53% (0.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06824892B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-ce03647b6b234a8da4d5ed859b007687 |
| Source note | uspto-grants-2004_11 |