HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 21105481, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Butoxybenzoic acid | HCID 72971 | — |
| Reactant | 4-(1,4-Dioxa-7-azaspiro[4,4]non-7-yl)phenylamine | HCID 21105432 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21105481 | HCID 21105481 | — |
Reaction Steps
4-Butoxybenzoic acid was reacted with 4-(1,4-dioxa-7-azaspiro[4,4]non-7-yl)phenylamine by method E. The resulting amide (0.25 g) in acetone (10 ml) was mixed with para-toluenesulfonic acid (monohydrate, 109 mg), and the mixture was refluxed for 8 hours. After addition of triethylamine (0.5 ml), the mixture was diluted with water and extracted with ethyl acetate. The organic phase was dried over magnesium sulfate and concentrated. The product with the molecular weight of 352.44 (C21H24N2O3); MS (ESI): 353 (M+H+) was obtained in this way.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07838547B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-7268cda35bf14d4c8bc7c5016462d2c5 |
| Source note | uspto-grants-2010_11 |