HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → Methyl 2-[2-Hydroxy-3-[N-[2-[N-(4-methylphenylsulfonyl)amino]ethyl]amino]propoxy]benzoate Oxalate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | Methyl 2-(oxiran-2-ylmethoxy)benzoate | HCID 279510 | — |
| Reactant | N-(2-Aminoethyl)-4-methylbenzenesulfonamide | HCID 301318 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 2-[2-Hydroxy-3-[N-[2-[N-(4-methylphenylsulfonyl)amino]ethyl]amino]propoxy]benzoate Oxalate | HCID 13732868 | — |
Reaction Steps
A solution of 2.15 of N-(2-aminoethyl)-p-toluenesulfonamide (0.1 mole) and 2.08 g of methyl 2-(2,3-epoxypropoxy)benzoate (0.01 mole) in 100 ml of methanol was stored at 25° C. for 4 hours. The methanol was then removed under reduced pressure, leaving an oil (NMR indicated only mono-alkylated product). The oil was then dissolved in 50 ml of methanol and an equimolar quantity of oxalic acid was added to the solution. 50 Ml of acetone was added, and the product crystallized upon refrigeration. The product was recrystallized from acetone/methanol (1:1) to yield 1.4 g of product which had a melting point of 165°-166° C. The elemental analysis (CHN) and NMR spectrum were consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04692446 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-9a56a270cf6c40819de273747a148323 |
| Source note | uspto-grants-1987_09 |