HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Trifluoromethyl)benzenesulfonyl chloride → HCID 86626020, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Trifluoromethyl)benzenesulfonyl chloride | HCID 2777399 | — |
| Reactant | HCID 86626018 | HCID 86626018 | — |
| Reactant | HCID 86626021 | HCID 86626021 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86626020 | HCID 86626020 | — |
Reaction Steps
0.792 g (3.065 mmol) of a 1:1 mixture trans-(7-amino-3,4,4a,5,10,10a-hexahydro-2H-benzo[g]quinolin-1-yl)-propan-1-one and trans-(8-amino-3,4,4a,5,10,10a-hexahydro-2H-benzo[g]quinolin-1-yl)-propan-1-one were dissolved in 20 ml pyridine. At 0-4° C., 0.75 g of 4-trifluoromethyl-benzene sulfonylchloride (3.066 mmol) were added, and the reaction stirred for 2 h under cooling. Pyridine was evaporated and the residue partitioned between 20% aqueous citric acid and diethylether. The aqueous layer was extracted twice with diethylether, the combined organic phases washed with 20% aqueous citric acid, dried over magnesium sulfate, filtered, and the solvent evaporated under reduced pressure to yield 1.327 g of the product. MSD: 467.1 g/mol
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08969552B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-9d1acc4f99a5483a8555709007ab1c94 |
| Source note | uspto-grants-2015_03 |