HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 87486712, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 642407-44-1 | HCID 10057607 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 87486712 | HCID 87486712 | 892.6% |
Reaction Steps
0.60 g (3.5 mmole) anhydrous tosylic acid was dissolved in possibly as little as ethanol. Then a solution of 0.55 g (0.38 mmole) N-(1-methylethyl)-2,3-dimethyl-2-butylamine in 10 mL anhydrous ether was added dropwise with stirring. The mixture was stood overnight, and then distilled off the solvent. The residue was washed thoroughly with anhydrous ethanol to give a colorless solid 1.07 g, mp 119-120° C. 1H-NMR(D2O, ppm) 0.96(d, 6H, 2CH3), 1.303(s, 6H, 2CH3), 1.36(d, 6H, 2CH3), 2.02-2.15(m, 1H, C(H), 2.401(s, 3H, CH3), 3.62-3.73(m, 1H, CH), 7.38(d,2H, 2Ar—H), 7.70(d,2H, 2Ar—H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07560473B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-4c8e56ae23b34f36aa297348ef341d31 |
| Source note | uspto-grants-2009_07 |