HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylamine → HCID 21099927, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylamine | HCID 1146 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | HCID 21099926 | HCID 21099926 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21099927 | HCID 21099927 | 95.9% |
Reaction Steps
A 1.2 g of 8-(4′-isopropylanilino)-1,5-dihydroxy-4-nitroanthraquinone and a 1.4 g of tosyl chloride were dissolved in 20 ml of dichloromethane, and a 1.0 ml of trimethylamine was added to the solution and allowed to react for 12 hours at room temperature under stirring. The reaction solution was extracted with adequate amounts of ethyl acetate and 1N-hydrochloric acid to separate into two layers. The extracted organic layer was dried with magnesium sulfate and concentrated. The obtained product was purified by silica gel chromatography to give a 2.0 g of 8-(4′-isopropylanilino)-4-nitro-1,5-bis(p-toluenesulfonyloxy)anthraquinone in a 94% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07220465B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-4a9cafc164254acea8606180d11c208d |
| Source note | uspto-grants-2007_05 |