HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-Cyclopropyloxyimino-2-(5-tritylamino-1,2,4-thiadiazol-3-yl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-cyclopropyloxyimino-2-(5-tritylamino-1,2,4-thiadiazol-3-yl)acetate | HCID 53744924 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Cyclopropyloxyimino-2-(5-tritylamino-1,2,4-thiadiazol-3-yl)acetic acid | HCID 54185678 | 74.7% |
Reaction Steps
A solution of ethyl 2-cyclopropyloxyimino-2-(5-tritylamino-1,2,4-thiadiazol-3-yl)acetate (syn isomer)(11 g) in a mixture of tetrahydrofuran (72 ml), methanol (72 ml) and 2N sodium hydroxide (72 ml) was stirred at ambient temperature overnight. The mixture was concentrated in vacuo. The residue was dissolved in a mixture of ethyl acetate and water and adjusted to pH 2 with 3N hydrochloric acid. The organic layer wad separated, washed with water and saturated aquious solution of sodium chloride, dried over magnesium sulfate, concentrated in vacuo, and triturated with petrolium ether to give 2-cyclopropyloxyimino-2-(5-tritylamino-1,2,4-thiadiazol-3-yl) acetic acid (syn isomer) (7.75 g) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04861769 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-2fb0e690f22146ab960d5e067ec40bb0 |
| Source note | uspto-grants-1989_08 |